| ROCHE DIAGNOSTICS OPERATIONS, INC. Patent applications |
| Patent application number | Title | Published |
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| 20120130062 | ENZYMATIC SYNTHESIS OF CARBA-NAD - The disclosure concerns the enzymatic synthesis of stable analogues of nicotinamide adenine dinucleotide NAD/NADH and nicotinamide adenine dinucleotide phosphate NADP/NADPH, the so-called “carba-NADs”, i.e. analogues of NAD/NADH or NADP/NADPH, respectively, comprising a carbacyclic sugar instead of ribose. | 05-24-2012 |
| 20120129181 | DETECTION OF BACTERIAL (MOLLICUTES) CONTAMINATION - The present disclosure provides a method and system for the PCR amplification of a target sequence which suppresses non-specific amplification products. The disclosure concerns the use of a primer pair optimized to amplify a nucleic acid of a contaminant in the background of genomic DNA of a first organism. When DNA from a second organism suspected for comprising the contaminant is subjected to the same PCR-based amplification reaction, detection sensitivity and specificity of the contaminant is enhanced when an amount of genomic DNA of the first organism is present in the amplification reaction. | 05-24-2012 |
| 20120125789 | ENZYME STABILIZATION IN ELECTROCHEMICAL SENSORS - The present invention relates to a composition for forming an electrode, an electrochemical sensor comprising the same, and a method for determining an analyte using the electrochemical sensor. | 05-24-2012 |
| 20120122594 | ANALYTICAL TEST APPARATUS COMPRISING A FRICTION CLUTCH - An analytic test instrument ( | 05-17-2012 |
| 20120122227 | GUIDED STRUCTURED TESTING KIT - A guided structured testing kit comprising a test strip container, a test strip meter, a testing protocol advisor, and at least one of diagnostic test strip is presented. The diagnostic test strip comprising a support element, a glucose reagent provided on the support element, and a glycemic context code provided on the support element. The glycemic context code can be machine-readable. The glycemic context code signals a glycemic context to a test strip meter, either upon insertion of the diagnostic test strip or by a user manually inputting the glycemic context into the test strip meter. A method for performing a guided structured test is also provided. | 05-17-2012 |
| 20120120388 | System for Performing Scattering and Absorbance Assays - An optical system for performing scattering and absorbance assays in clinical diagnostics comprises a light source for emitting collimated light parallel to an optical axis in an optical path, a sample holding unit comprising at least one sample holding position located in the optical path and an optical detector for measuring light transmitted through a sample located in a sample holding position. The optical system further comprises an adjustable light angle selector adjusted to prevent light transmitted through the sample and diverging from the optical axis with an angle greater than a certain value from reaching the detector when a scattering assay is performed, and wherein the light angle selector is adjusted to allow light transmitted through the sample and diverging from the optical axis with an angle smaller than a certain value to reach the detector when an absorbance assay is performed. | 05-17-2012 |
| 20120116437 | LANCET - The invention relates to a lancet having a flat shaft ( | 05-10-2012 |
| 20120116436 | SAFETY LANCET - A lancet, a lancing device, a method of loading a lancet into a lancing device, and methods of manufacturing and utilization thereof are disclosed. The lancet may have a needle, a body attached to the base of the needle, arm members attached to the body, and a tip cover attached to the arm members and slidably attached to the needle, wherein at least one of the tip cover and the body is selectively moveable between an operative configuration and a protective configuration. The lancing device may have a lancet holder having surfaces which retain the lancet. The method of loading a lancet may involve providing the lancet in a protective configuration and inserting the lancet into a lancet holder of the lancing device, such that the tip cover or the body is selectively moveable between an operative configuration and a protective configuration. | 05-10-2012 |
| 20120116347 | THERAPY DELIVERY SYSTEM HAVING AN OPEN ARCHITECTURE AND A METHOD THEREOF - A therapy delivery system having an open architecture and method of providing thereof are disclosed. The present invention provides a therapy dosage module having a control algorithm that can be replaced with a predefined or independently defined control algorithm. The tools necessary to create and test such control algorithms in the therapy dosage module in a simulated environment before implementing it in a live therapy system are also disclosed. | 05-10-2012 |
| 20120116250 | TEST UNIT FOR USE IN A TEST DEVICE AND TEST SYSTEM - The invention concerns a test system comprising a test device which has a lancing drive and an optical measuring device, and at least one test unit that is inserted into the test device as a disposable article, preferably in a magazine. According to the invention it is proposed that the measuring device can be directly coupled to a detection element of the test unit by means of an optics adapter on the device side, where a free end of the spring-loaded optics adapter lies against the detection element in a force-locking manner. | 05-10-2012 |
| 20120109531 | ANALYSIS SYSTEM FOR ANALYZING BIOLOGICAL SAMPLES - An analysis system for analyzing biological samples is disclosed, and which may comprise two or more analysis system components for performing an analysis. A sample workflow manager and an instrument manager coupled to the sample workflow manager may be coupled to the system components for receiving a process status from the system components, wherein the sample workflow manager provides at least one preconfigured processing route to the instrument manager in accordance with the process status. The instrument manager may comprise a memory for storing the preconfigured processing route, wherein the instrument manager is adapted for receiving a test order for analyzing the biological sample using the system components, and wherein the instrument manager is adapted for generating commands for controlling a transport device for transporting the biological sample in accordance with the test order and the at least one preconfigured processing route. | 05-03-2012 |
| 20120096451 | FIRMWARE UPDATE IN A MEDICAL DEVICE WITH MULTIPLE PROCESSORS - The present disclosure describes a handheld diabetes management device that implements a failsafe firmware upgrading protocol to reduce required user interaction and risk of device downtime. The general processing module executes first software from nonvolatile memory. The general processing module receives second software from an external port and writes the second software to the nonvolatile memory. Based on an upgrade signal, the general processing module switches execution from the first software to the second software, evaluates proper operation of the general processing module, and switches execution back to the first software from the second software when proper operation of the general processing module using the second software is not detected. A communications module, in electrical communication with the general processing module, stores third software and executes the third software. The general processing module receives fourth software from the external port and replaces the third software with the fourth software. | 04-19-2012 |
| 20120095774 | METADATA TAGGING SYSTEM FOR A DIABETES MANAGEMENT SYSTEM OF DEVICES - A diabetes management system having a reliable data management scheme is disclosed. The system comprises a plurality of devices, each device performing a different function relating to treatment of diabetes. Each device has a device identifier and each device generates data records relating to the function of the device. Each device includes a metadata generator configured to generate a metadata tag for a data record generated by the device. A metadata tag includes the device identifier of the corresponding device, a record identifier, and a source identifier indicating whether the record was originated by a human or the device. The system further includes a diabetes management device in communication with the plurality of devices and configured to manage records received from the plurality of devices. When a first device of the plurality of devices generates a new record to be communicated to the diabetes management device, the metadata generator of the first device generates a new unique record identifier and a new metadata tag based on the new unique record identifier and the device identifier of the first device, and the first device propagates the new record and the new metadata tag to the second device. | 04-19-2012 |
| 20120095773 | HANDHELD DIABETES MANAGEMENT DEVICE FOR OBTAINING THREE DAY BLOOD GLUCOSE PROFILE - A method is disclosed for managing a three day profile blood glucose (bG) measurements that are provided by a user using a handheld diabetes management device. The method may involve configuring a database carried by the device to store a plurality of bG test values input by a user for each day of a three day test period. The bG test values are required to be provided by the user in accordance with a predetermined plurality of differing acceptance time windows during each day of the three day test period. If two or more windows are open concurrently when a given bG test value is obtained, the system allows the user to select the appropriate time window that the given bG test value should be associated with. A processing subsystem of the device determines if at least a predetermined minimum plurality of the stored bG test values has been provided by the user during the predetermined plurality of differing acceptance time windows for each day of the three day test period and, if so, the processing subsystem accepts the bG test values provided by the user when compiling results for a three day bG profile. | 04-19-2012 |
| 20120095691 | HANDHELD DIABETES MANAGEMENT DEVICE HAVING TESTING IN PAIRS BLOOD GLUCOSE TEST - A method for conducting a Testing In Pairs (TIPs) blood glucose (bG) test using a handheld diabetes management device carried by a user. A processing subsystem of the device implements a software module for managing the TIPs test. The software module generates a plurality of predetermined acceptance time windows corresponding to different user defined events. The processing subsystem can identify specific ones of a plurality of bG test values read by the device that are obtained during the predetermined bG acceptance time windows, and which are identified as being related pairs of accepted bG test values that correspond to specific ones of the user defined events. The related pairs of accepted bG test values can then be stored in a database. | 04-19-2012 |
| 20120095393 | USE OF A HANDHELD MEDICAL DEVICE AS A COMMUNICATIONS MEDIATOR BETWEEN A PERSONAL COMPUTER-BASED CONFIGURATOR AND ANOTHER NETWORKED MEDICAL DEVICE - A handheld diabetes managing device that provides a secure and efficient communication link between an insulin pump and an external computing device. The handheld diabetes managing device can include a blood glucose meter, a processor and first and second communication modules. The handheld diabetes managing device can be configured to deliver data between an insulin pump and an external computing device over a secure communication path without a direct communication link between the insulin pump and the external computing device. The secure communication path can include a first secure bidirectional communication link between the handheld diabetes managing device and the insulin pump and a second secure bidirectional communication link between the handheld diabetes managing device and the external computing device. | 04-19-2012 |
| 20120095318 | HANDHELD DIABETES MANAGEMENT DEVICE WITH BOLUS CALCULATOR - A method for monitoring blood glucose (bG) levels of a diabetic user. The method may be implemented on a non-transitory computer readable medium adapted to run on a processing subsystem, the processing subsystem forming a portion of a handheld diabetes management device for monitoring the bG levels of a diabetic user and determining a correction bolus to be provided to the user. The method may comprise using a memory to store information in a plurality of different time blocks. The information may include a plurality of differing user defined health events that each include a predetermined associated percentage value set by the user by which a correction bolus calculation will be modified to account for one of an increase or a decrease in insulin associated with each one of the defined health events. The processing subsystem may be used to communicate with the memory and to obtain the information and to calculate therefrom the correction bolus. | 04-19-2012 |
| 20120095317 | COMMUNICATION PROTOCOL THAT SUPPORTS STRUCTURED COLLECTION PROCEDURES USED IN DIABETES CARE - A computer-implemented diabetes management system is provided for configuring a structured collection procedure implemented on a collection device having a meter that measures the concentration of glucose in blood. The system includes: a collection application that executes a structured collection procedure for obtaining measurement data from the meter and provides access to the measurement data via a communication protocol defined in accordance with IEEE standard 11073-20601; a configuration application that accesses and manipulates the parameters of the structured collection procedure using a set of action commands, where the set of action commands are defined in compliance with the communication protocol; and a collection interface that receives an action command from the configuration application, executes the received action command and issues a response command in response thereto, where the response command is defined in compliance with the communication protocol. | 04-19-2012 |
| 20120095315 | CONFIGURATION OF BLOOD GLUCOSE METER INTERFACES - A handheld diabetes management device includes a blood glucose measurement engine that measures a blood glucose level of a patient. The device includes a physical port that is exposed at an exterior of the device. The device includes a processing module that includes first, second, and third physical interfaces that are internal to the device. The device includes a multiplexing module that alternatively connects the physical port to one of the first, second, and third physical interfaces of the processing module. The processing module selectively operates the first physical interface using first and second modes. When an external host is connected to the physical port, the processing module selectively transfers information based on the blood glucose level to the external host using the first mode. When the external host is connected to the physical port, the processing module selectively provides file access to the external host using the second mode. | 04-19-2012 |
| 20120095314 | HANDHELD DIABETES MANAGEMENT DEVICE HAVING A DATABASE MANAGEMENT SYSTEM - A handheld diabetes management device having a database management system is disclosed. The device comprises a plurality of input modules, including a blood glucose reader, a user interface, a communications interface, and a continuous blood glucose input module. The input modules output data used to generate data records of different record types. The device further comprises N databases, each database having a different frequency range associated thereto, wherein the new record is stored in a particular database of the N databases based on the frequency range of the particular database and the frequency of the particular record type, and N is an integer greater than 1. The device further includes a database operation module that performs database operations on the N databases. The database management system provides increased reliability in the keeping of records on which medically important decisions are made. | 04-19-2012 |
| 20120095313 | MEDICAL DEVICES THAT SUPPORT ENHANCED SYSTEM EXTENSIBILITY FOR DIABETES CARE - A medical device or medical software is provided that supports system extensibility for diabetes care. The medical device or software is comprised of an application and particular data structures that support diabetes care. The data structures include: a patient class that has attributes and methods associated with a person receiving medical treatment for diabetes; a patient log class that has a composition relationship with the patient class and attributes and methods that log actions taken by the patient; a treatment plan class that has a composition relationship with the patient class and attributes and methods that define a series of planned actions related to medical treatment of the patient; and an adherence class that has a composition relationship with the patient log class and attributes and methods define relationships between actions planned for the patient and actions taken by the patient. The application instantiates an object from at least one of the patient log class, the adherence class and the treatment plan class, having only external-to-the-composition knowledge of which objects are instantiated, and performs a function using the instantiated object. | 04-19-2012 |
| 20120095312 | POWER MANAGEMENT FOR A HANDHELD MEDICAL DEVICE - A system for managing power consumption of a handheld diabetes management device and limiting effects of temperature on operations performed by the handheld diabetes management device comprises a blood glucose measuring module, a temperature sensing module, and a power management module. The blood glucose measuring module selectively measures blood glucose in a blood sample and generates a status signal indicating a status of operation of the blood glucose measuring module. The temperature sensing module senses an internal temperature of the handheld diabetes management device and estimates an ambient temperature external to the handheld diabetes management device. The power management module deactivates one or more components of the handheld diabetes management device based on the status of operation of the blood glucose measuring module when the internal temperature of the handheld diabetes management device exceeds a threshold temperature. The power management module deactivates the blood glucose measuring module when the ambient temperature is greater than a first predetermined threshold or less than a second predetermined threshold. | 04-19-2012 |
| 20120095311 | COEXISTENCE OF MULTIPLE RADIOS IN A MEDICAL DEVICE - A handheld diabetes management device having a plurality of communication modules for communicating with a plurality of medical devices via a shared antenna or multiple antennas, where the handheld diabetes management device includes a first communication module, a second communication module, and an arbitration module. The first communication module selectively communicates in a first frequency band with an insulin infusion pump external to the handheld diabetes management device via a first antenna using a first wireless communication protocol. The second communication module selectively communicates in the first frequency band with a continuous glucose monitor external to the handheld diabetes management device via a second antenna or the first antenna using a second wireless communication protocol. The arbitration module grants permission to communicate to the first communication module and denies permission to communicate to the second communication module when the first and second communication modules request permission to communicate concurrently. | 04-19-2012 |
| 20120095310 | TIME BLOCK MANIPULATION FOR INSULIN INFUSION DELIVERY - The present teachings provide a system for modifying insulin therapy support parameters such as warning limit data and time block data on a hand-held diabetes management device. The system can include a graphical user interface module that creates a graphical user interface having a plurality of bar structures positionable on or between a first line that indicates an upper limit and a second line that illustrates a lower limit. Each of the bar structures can have a first side that indicates a start time of a time window opposite a second side that indicates an end time of the time window and a third side that indicates a lower target value for a blood glucose level opposite a fourth side that indicates an upper target value for the blood glucose level. The bar structures, the first line and the second line can be adjustable by a user input. | 04-19-2012 |
| 20120095309 | UPDATABILITY OF STRUCTURED BLOOD GLUCOSE TESTS PERFORMED ON HANDHELD DIABETES MANAGEMENT DEVICES - A method of improving updatability of entry, adherence, and exit criteria stored in memory of a handheld diabetes management device, the method includes: providing the handheld diabetes management device with a blood glucose (bG) measurement engine that measures a bG level in a sample of blood of a user and that generates sample data indicative of the bG level; providing the handheld diabetes management device with the memory and a touchscreen display; providing the handheld diabetes management device with a processor module that is in communication with the bG measurement engine, the touchscreen display, and the memory; storing firmware that is executable by the processor module for performing operations to carry out a structured bG test in a non-modifiable portion of the memory; and storing the entry, adherence, and exit criteria in a modifiable portion of the memory. | 04-19-2012 |
| 20120094370 | BLOOD GLUCOSE TEST INSTRUMENT KIT HAVING MODULAR COMPONENT PARTS - A blood glucose test instrument kit having modular component parts capable of being assembled into a plurality of different handheld blood glucose test instruments is disclosed. The kit comprises the combination of an interconnection platform adapted to connect to a collection of interoperable modules. The collection of interoperable modules including: a plurality of different measurement engine modules, at least one user interface module, at least one power supply module. A handheld blood glucose test instrument is assembled by the interconnection to the interconnection platform of at least one measurement engine module, at least one user interface module, and at least one power supply module. The inter-module communication among the modules connected thereto to achieve enhanced glucose test instrument reliability by effecting at least one reliability protocol selected from a group of reliability protocols. | 04-19-2012 |
| 20120093315 | DIABETES CARE KIT THAT IS PRECONFIGURED TO ESTABLISH A SECURE BIDIRECTIONAL COMMUNICATION LINK BETWEEN A BLOOD GLUCOSE METER AND INSULIN PUMP - A diabetes care kit for providing diagnostics and therapy that is preconfigured to reduce initial setup by a user. The kit can include a handheld diabetes managing device and insulin pump. The handheld diabetes managing device and insulin pump can each be preloaded with an encryption key such that the handheld diabetes managing device and the insulin pump are paired and a secure bidirectional communication link exists between the handheld diabetes managing device and the insulin pump. | 04-19-2012 |
| 20120093311 | EFFICIENT PROCEDURE FOR PAIRING MEDICAL DEVICES FOR WIRELESS COMMUNICATION WITH LIMITED USER INTERACTION - A method for pairing a handheld diabetes managing device with an insulin pump for secure wireless communication with limited user interaction. A pump identification code that uniquely identifies the insulin pump can be displayed on the diabetes managing device and insulin pump. The diabetes managing device can receive an insulin pump selection input that selects the pump identification code corresponding to the insulin pump. The diabetes managing device and insulin pump can generate and display a first verification string and second verification string, respectively. Confirmation inputs corresponding to the first verification string matching the second verification string can be received at both the insulin pump and the diabetes managing device such that a secure bidirectional communication link between the diabetes managing device and the insulin pump is established. | 04-19-2012 |
| 20120092812 | HANDHELD DIABETES MANAGER WITH TOUCH SCREEN DISPLAY - A handheld diabetes manager having a blood glucose measurement engine comprises a housing having a blood glucose measuring engine and a printed circuit board disposed in the housing. A touch screen can be coupled to the housing. The touch screen can have a transparent portion surrounded by a non-transparent portion. The non-transparent portion can have adhesive thereon that seals the touch screen to the housing. A flexible connector can electrically connect at least two independent electrical leads between the touch screen and the printed circuit board. An antenna assembly can be disposed in the housing and comprise a molded carrier, a conductive portion on the molded carrier and a speaker. The conductive portion can be electrically connected to the printed circuit board and be configured to receive a radio signal. The carrier can include a recess that receives the speaker and is configured to project sound from the speaker. | 04-19-2012 |
| 20120089893 | Management Method And System For Implementation, Execution, Data Collection, and Data Analysis Of A Structured Collection Procedure Which Runs On A Collection Device - A collection device for performing a structured collection procedure may include a processor that executes program instructions communicably coupled to at least one memory. The processor can initiate a schedule of events of the structured collection procedure upon one or more entry criterions being met and segregate the at least one memory into a primary data store and a secondary data store. The processor can write structured patient data collected in accordance to the schedule of events to the secondary data store. The processor can transform a relevant portion of the structured patient data into an evaluated data object. The processor can generate a data abstraction based in part upon the evaluated data object. The processor can link the primary data store and the secondary data store with the data abstraction. | 04-12-2012 |
| 20120078221 | METHODS AND SYSTEMS FOR ADJUSTING AN INSULIN DELIVERY PROFILE OF AN INSULIN PUMP - Systems and methods are disclosed for adjusting the delivery times of an insulin delivery profile of an insulin pump, wherein the insulin pump is operable to automatically deliver insulin to a person having diabetes based on an operating time of the internal clock and a delivery time of an insulin delivery profile. The method may comprise receiving a local time zone time from an external local clock, determining whether the operating time of the internal clock differs from the local time zone time by at least a first predetermined amount of time, requesting the person provide a time adjustment value when the operating time of the internal clock differs from the local time zone time by at least the first predetermined amount of time, receiving the time adjustment value from the person, and adjusting the delivery times of the insulin delivery profile based on the time adjustment value when received. | 03-29-2012 |
| 20120071791 | TEST DEVICE IN PARTICULAR FOR BLOOD SUGAR TESTS - The invention concerns a test device, in particular for blood sugar tests, comprising a lancing element which is provided with a lancing component for producing a skin puncture, and a protecting element shielding the lancing element at least in the area of the lancing component. According to the invention it is proposed that the lancing element has a collecting structure for collecting body fluid from the skin puncture and that the protecting element comprises a protecting foil to cover the collecting structure and a holding body for holding the protecting foil on the lancing element. | 03-22-2012 |
| 20120066185 | SYSTEM AND METHOD FOR DATABASE INTEGRITY CHECKING - A method is disclosed for checking the integrity of a database through a test of database integrity information provided in the database and integrity information provided external to the database. The integrity information may be provided in a configuration file. | 03-15-2012 |
| 20120064615 | TEST ELEMENT FOR DETECTING AN ANALYTE IN A SAMPLE - The invention relates to a test element for detecting at least one analyte in a sample, in particular for detecting at least one metabolite in a bodily fluid. The test element comprises at least one test field with a test field surface. The test field comprises at least one detection reagent that is adapted to undergo a detectable reaction in the presence of the analyte. The test element further comprises at least one distribution element that has at least one distribution surface facing the test field surface. Between the distribution surface and the test field surface is at least one capillary gap, wherein the capillary gap is adapted to allow a layer of the sample with a layer thickness of no more than 50 μm to form within the capillary gap. | 03-15-2012 |
| 20120063970 | METHOD FOR PRODUCING AN ANALYTICAL MAGAZINE - A method for producing an analytical magazine is proposed. The analytical magazine is designed to receive a plurality of analytical aids in a plurality of chambers. The method comprises the following steps: providing at least one first component of the analytical magazine, wherein the first component comprises a plurality of receptacles; providing a plurality of analytical aids, wherein the analytical aids are connected to one another and preferably oriented with respect to one another by at least one holding element; introducing the analytical aids into the receptacles; and separating the analytical aids from the holding element. | 03-15-2012 |
| 20120059231 | DEVICE FOR PERFORMING AT LEAST ONE MEDICAL FUNCTION - A device for performing at least one medical function on a user is proposed. The device has at least one medical functional element that is designed to perform the medical function. The medical function is selected from a diagnostic, a therapeutic and a surgical function. The device has at least one evaluation and control part that comprises at least one actuation component for controlling the medical function. The evaluation and control part has at least one casing and at least one battery receptacle. The battery receptacle comprises at least one electrical energy reservoir, more particularly at least one battery. The battery receptacle is designed to be opened irreversibly by the user for removing the energy reservoir. | 03-08-2012 |
| 20120041340 | LANCING SYSTEM - The invention relates to a lancing system, comprising test elements, lancing elements, test elements each assigned to a lancing element and a hand-held device comprising a holder, which during a puncture holds a lancing element and a test element assigned to it, a lancing drive, which during a puncture moves the holder out of a starting position into a piercing position and back into the starting position, a light-sensitive sensor for analyzing a body fluid sample taken up by a test element, and a light source for illuminating the test element. According to the invention, the sensor is disposed in a housing, the outside of which the holder touches in the starting position. | 02-16-2012 |
| 20120041339 | SPACE-SAVING MAGAZINING OF ANALYTICAL AIDS - An analytical magazine is proposed, which comprises a plurality of analytical aids accommodated in chambers. The analytical magazine is arranged to be accommodated in at least two orientations in an analytical system. The analytical magazine is furthermore arranged to provide the analytical system, in the orientations, in each case with a plurality of analytical aids. At least one sampling movement can be executed by means of the analytical aids. The analytical magazine is arranged to make a remagazining of the analytical aids possible. | 02-16-2012 |
| 20120039772 | TEST ELEMENT MAGAZINE HAVING COVERED TEST FIELDS - An analytic magazine is proposed, which comprises at least one chamber with at least one analytic aid. The analytic aid comprises at least one test element for detecting at least one analyte in a sample of a bodily fluid. The test element has at least one test field with at least one test chemical. The test field is at least partly arranged within the chamber, wherein at least one wall of the chamber at least partly covers the test field and at least partly delimits a test-field surface that is accessible from the chamber. | 02-16-2012 |
| 20120022345 | LANCET HAVING CAPILLARY CHANNEL AND STERILE PROTECTION ELEMENT AND METHOD FOR PRODUCING SUCH A LANCET - Lancets comprising a piercing element for puncturing the skin of a patient, a test region containing detection reagents for determining an analyte concentration of a body fluid sample, a capillary structure arranged in the piercing element for transporting a body fluid sample to the test region, and a sterile protection element, which encloses the tip of the piercing element. The capillary structure is blocked in a section surrounded by the sterile protection element. Also provided are methods for producing a lancet, comprising: producing a piercing element, which on the upper side has an upwardly open capillary structure; covering a section of the upper side of the piercing element and blocking the capillary channel in this section using a first material; covering a section of the underside using a second material; sterilizing the piercing element; and attaching a test region containing detection reagents to the piercing element. | 01-26-2012 |
| 20120022344 | INSERTION SYSTEM AND INSERTION DEVICE - An insertion system having a base unit for placing on the body of a patient and an insertion device that can be coupled to the base unit, wherein the insertion device comprises an insertion needle holder for holding an insertion needle and a drive mechanism for displacing the insertion needle holder in a pricking direction. According to the invention, the insertion device comprises a locking mechanism causing locking of the drive mechanism in an active state and being set to an inactive state in which the locking is released by coupling the insertion device to the base unit. | 01-26-2012 |
| 20120017945 | Wash Element, Wash Station and Process for Washing Reusable Fluid Manipulators - A wash element for washing one or more reusable fluid manipulators is provided comprising at least one nozzle for connection to a fluid pump to generate a fluid jet and at least one deflector surface positioned to deflect the fluid jet towards a washing zone for receiving at least a portion of the fluid manipulator. The deflector surface is being shaped to broaden the fluid jet. The invention further relates to a wash station having a cavity provided with one or more wash elements. The invention yet further relates to an automated system for manipulating fluids comprising at least one wash station and a controller set up to control washing the fluid manipulator. In a process for washing the reusable fluid manipulator at least a portion of the fluid manipulator is moved in a washing zone, a fluid jet of washing fluid is generated and directed onto a deflector surface shaped to broaden and deflect the fluid jet towards the washing zone. | 01-26-2012 |
| 20120011125 | MANAGEMENT METHOD AND SYSTEM FOR IMPLEMENTATION, EXECUTION, DATA COLLECTION, AND DATA ANALYSIS OF A STRUCTURED COLLECTION PROCEDURE WHICH RUNS ON A COLLECTION DEVICE - Method embodiments for performing a structured collection protocol by utilizing a collection device comprise collecting one or more sampling sets of biomarker data, wherein each sampling set comprises a sufficient plurality of sampling instances recorded over a collection period. The methods further include determining compliance with adherence criteria for the sampling instances, wherein noncompliance with adherence criteria is recorded as an adherence event, classifying sampling instances as primary samples or secondary samples, wherein primary samples, which do not have corresponding recorded adherence events, are sampling instances utilized in the calculations performed by the processor that yield therapy results for a diabetic person, and secondary samples are sampling instances not utilized in the calculations, unless one or more secondary samples are promoted to primary samples, and performing at least one additional task if one or more sampling instances is a primary sample with a corresponding recorded adherence event. | 01-12-2012 |
| 20120010482 | INSERTION SYSTEM - An insertion system for inserting a sensor into fatty tissue, comprising an insertion device and an insertion needle containing a sensor, wherein the insertion device comprises a holder for the insertion needle, and a piercing mechanism so as to move the holder, with the needle held by the same, in a feed direction for a puncture. The piercing mechanism changes the feed direction during the puncture so that, at the end of the puncture, an insertion needle held by the holder is oriented obliquely or perpendicular to the initial feed direction. Also provided are methods for controlling a needle moved by an insertion device. | 01-12-2012 |
| 20120009102 | FOLDED CARRIER TAPE HAVING CONSUMABLE ELEMENTS - The invention relates to a carrier tape which carries a plurality of consumable elements for a system for determining an analyte concentration of a human or animal bodily fluid and is folded into a stack. According to the invention, the consumable elements are disposed on the carrier tape in groups, wherein the distance between adjacent groups in the longitudinal direction of the carrier tape is greater than that between adjacent consumable elements within a group. | 01-12-2012 |
| 20120006105 | SYSTEM AND METHOD FOR ANALYZING A BODY FLUID - The invention concerns a system for analyzing a body fluid comprising a collecting element which receives the body fluid in a reservoir, a test element designed to detect an analyte in the body fluid, a transfer device for making a fluidic connection between the collecting element and the test element, and a detection unit which detects an analyte-specific measurement signal on the test element during a measurement interval. According to the invention it is proposed that the transfer device always brings the test element into contact with the body fluid located in the reservoir during the measurement interval and that the transfer device is configured to physically separate the test element and the collecting element from one another after the measurement interval. | 01-12-2012 |
| 20120004853 | Analysis System And Computer Implemented Method For Analyzing Biological Samples - Analysis system and computer implemented method for analyzing biological samples are disclosed. The system has at least one analyzer for performing an analysis and a decision unit being operable to determine in response to the receipt of the analysis request whether results obtained from performing the analysis on the sample indicated in the analysis request are valid. This determination is executed by retrieving the meta information assigned to the sample and by applying the at least one condition on the meta information and wherein the at least one applied condition has at least a condition on whether the sample allows a valid analysis on the sample, and wherein the decision unit returns the decision that the analysis exercised on the indicated sample will return a valid result in case the conditions of the condition set are met by the sample. | 01-05-2012 |
| 20120000299 | Method and device for providing blood constituents - A metering capillary and method for providing at least one defined volume of a target constituent of a sample is provided, the method comprising providing at least one metering capillary having at least two openings; at least partly filling the metering capillary with the sample; carrying out a constituent separation for the at least partial separation of at least two constituents of the sample inside the metering capillary; and dividing the metering capillary into at least two partial pieces, wherein at least one of the partial pieces contains the defined volume of the target constituent. | 01-05-2012 |
| 20110314903 | BODY FLUID TESTING DEVICE - Body fluid testing device for analyzing a body fluid comprises a test media tape adapted to collect the body fluid. The test media tape comprises a tape and test media portions. A free tape portion without test medium is located between successive test media portions. The testing device further comprises a supply portion. The supply portion comprises a housing in which uncontaminated test media tape is contained. The housing further has an opening for withdrawing test media tape from the housing. The testing device further has a sealing means for closing the opening against the surrounding. A free tape portion of the test media tape is located between a wall of the housing and the sealing means when the sealing means closes the opening. Further aspects concern a test media cassette with sealing means and a method for providing test media while holding them sealed against humidity during onboard storage. | 12-29-2011 |
| 20110313674 | INSULIN OPTIMIZATION SYSTEMS AND TESTING METHODS WITH ADJUSTED EXIT CRITERION ACCOUNTING FOR SYSTEM NOISE ASSOCIATED WITH BIOMARKERS - Embodiments of a testing method for optimizing a therapy to a diabetic patient comprise collecting at least one sampling set of biomarker data, computing a probability distribution function, a hazard function, a risk function, and a risk value for the sampling set of biomarker data wherein, wherein the probability distribution function is calculated to approximate the probability distribution of the biomarker data, the hazard function is a function which yields higher hazard values for biomarker readings in the sampling set indicative of higher risk of complications, the risk function is the product of the probability distribution function and the hazard function, and the risk value is calculated by the integral of the risk function, minimizing the risk value by adjusting the diabetic patient's therapy, and exiting the testing method when the risk value for at least one sampling set is minimized to an optimal risk level. | 12-22-2011 |
| 20110313673 | METHODS AND APPARATUS FOR DECENTRALIZED DIABETES MONITORING - Methods for decentralized monitoring of a progression of a diabetic state of a patient include contemporaneously obtaining an initial set of venous blood samples and an initial set of capillary blood samples after a standardized metabolic challenge from the patient in a centralized setting, wherein the diabetic state is diagnosed using the initial set of venous blood samples and a first test baseline is established by correlating the initial set of capillary blood samples with the initial set of venous blood samples, implementing a therapy, performing decentralized testing after reaching a target event, wherein a status test is obtained from a status set of capillary blood samples obtained from the patient after a subsequent standardized metabolic challenge, and comparing the status test with the first test baseline to determine an effectiveness of the therapy. | 12-22-2011 |
| 20110293475 | Analyzer For Performing Medical Diagnostic Analysis - Embodiments of an analyzer for performing medical diagnostic analysis of biological samples are disclosed. In one embodiment, the analyzer may have a first and at least a second disk-shaped cuvette conveyor each having an array of cuvette holders, a first drive unit for rotating the first cuvette conveyor about a rotation axis, and a second drive unit for rotating the second cuvette conveyor about the rotation axis. The operation of the second drive unit is independent from the operation of the first drive unit. The first cuvette conveyor and the second cuvette conveyor are spaced from each other in an axial direction along the rotation axis and with an air gap between them. The cuvette holders of the first cuvette conveyor and the cuvette holders of the second cuvette conveyor are adapted for holding cuvettes having the same shape and dimensions. | 12-01-2011 |
| 20110282244 | TEST STRIP DEVICE AND METHOD FOR ANALYZING A BODY FLUID - The invention concerns a test tape device for analyzing a body fluid having a carrier tape ( | 11-17-2011 |
| 20110282174 | ANALYSIS DEVICE WITH USER-FRIENDLY MENU CONTROLS - An analysis device is proposed for detecting an analyte in a liquid sample, in particular for detecting glucose in a bodily fluid. The analysis device comprises at least one control element, which is configured to provide a function menu with at least two menu items. The analysis device further comprises at least one adjustable selector element, in particular a mechanically adjustable selector element, which can be adjusted by a user to at least two different selection positions. The selector element is configured to remain in the adjusted selection position after being adjusted. The control element is configured to select a menu item corresponding to the adjusted selection position. The analysis device further comprises at least one operating element. At least one parameter in the selected menu item can be influenced by the user via the operating element. | 11-17-2011 |
| 20110278321 | HERMETICALLY SEALED TEST STRIP CONTAINER - A test strip container comprising a housing defining a cavity having a dispensing wall, a housing inlet, and a dispensing outlet is presented. The container may also comprise a lid mounted movably on the housing to define a primed position and an unprimed position therebetween. A cartridge may be provided within the cavity and holding a plurality of test strips. The cartridge may have a plunger entrance seal and a strip exit seal. A biasing member may be disposed within the cartridge urging the plurality of test strips towards the dispensing wall to be aligned with the dispensing outlet. A plunger may be provided, and oriented to open the plunger entrance seal through the housing inlet when the lid is in the primed position, and to urge a single test strip from the plurality of test strips through the strip exit seal of the cartridge and the dispensing outlet of the housing when the lid is transitioned from the primed position to the unprimed position. | 11-17-2011 |
| 20110270129 | INSTRUMENT AND SYSTEM FOR PRODUCING A SAMPLE OF A BODY LIQUID AND FOR ANALYSIS THEREOF - Instrument for producing a sample of body liquid for analysis by piercing the skin with a lancing element having a skin piercing tip. The instrument has a housing and a lancing drive for driving a lancing element connected thereto in a puncturing movement. A pressure ring surrounds a skin contact opening and is adapted for pressing against the skin. The skin contact opening has an opening area corresponding to a circle with a diameter of at least 1.5 mm and at most 4 mm, and the instrument comprises a pressing force control device for controlling the pressing force between the pressure ring and the skin at the time of triggering the puncturing movement, to be at least 3 N. | 11-03-2011 |
| 20110263039 | LIQUID CONTAINER WITH VARIABLE EXTRACTION CHIMNEY - A liquid container having a top opening, a base, and an extraction chimney which extends into the container and which is in alignment with the top opening is presented. The extraction chimney is intended for the withdrawal of liquid by a liquid-withdrawal element that is introduced into the liquid container through the extraction chimney. The extraction chimney has a liquid-permeable zone in its bottom region, adjacent to the liquid container base. The liquid permeability of the liquid-permeable zone of the extraction chimney can be adjusted between a setting for minimal liquid permeability and a setting for greater liquid permeability. The extraction chimney can be adjusted while the extraction chimney remains in the liquid container. | 10-27-2011 |
| 20110263006 | INTEGRATED TEST STRIP CONTAINER WITH RETAINING INSERT - A blood glucose meter for providing easy access to test strips and measuring blood glucose, a disposable and removable cartridge for providing easy access to test strips, and methods of manufacturing and utilization thereof are disclosed. The blood glucose meter for providing easy access to test strips and measuring blood glucose has a disposable and removable cartridge, a retaining member which releasably retains the test strips in a stacked configuration, and a housing. The disposable and removable cartridge has a rigid lid attached to a flexible body. | 10-27-2011 |
| 20110262303 | DEVICE FOR ANALYZING SAMPLES - Embodiments directed to a device for analyzing samples administered from a sample vessel are disclosed. One embodiment may comprise a central unit having a supply of reaction vessels and a sampling unit by which at least part of a sample is transferred from one of the sample vessels into the reaction vessel; at least one analytical unit having a plurality of reagent vessels; a transport unit which transports at least part of the reaction vessels from the central unit to the analytical unit such that the analytical unit supplies the reagent from the reagent vessels into the reaction vessel for triggering a reaction between the sample and the reagent; and at least one measuring unit provided in the analytical unit which measures the physical property of the sample held in the reaction vessel. | 10-27-2011 |
| 20110250695 | METHOD, STRUCTURE, DEVICE, KIT AND SYSTEM FOR THE AUTOMATED ANALYSIS OF LIQUID SAMPLES - A method for the automated analysis of liquid samples using at least one microfluidic structure is disclosed as well as microfluidic structures, a device having at least one of the microfluidic structures, a kit and a system including such microfluidic device. In one embodiment, the method may comprise: transferring said sample into a first fluid reservoir which is in fluid communication with a second fluid reservoir by a flow channel; spinning said microfluidic structure so as to transport said sample into one or more dead-end recesses or chambers; transferring a control fluid into the structure which generates a barrier to flow and diffusion of said sample contained in said one or more dead-end recesses or chambers; and analyzing said sample contained in said one or more dead-end recesses or chambers. | 10-13-2011 |
| 20110250093 | METHOD FOR PRODUCING A MAGAZINE BY INJECTION MOLDING, AND A MAGAZINE FOR AN ANALYSIS DEVICE - Method for the injection-molding production of a magazine having a plurality of chambers, separated by partition walls, including an outer wall formed by an outer wall of the magazine. The method uses a casting mold having an outer wall channel corresponding to the outer wall of the magazine, and partition wall channels corresponding to the partition walls, and a gate opening. A plurality of partition wall channels extend from the gate opening to the outer wall channel. The method comprises injecting a plastic compound into the gate opening. The plastic compound flows from the gate point to the partition wall channels into the outer wall channel. The plastic compound streams have a differing flow speed in alternating partition wall channels so a joint line, which is aligned with a partition wall channel, forms on the outer side of the outer wall channel. | 10-13-2011 |
| 20110246242 | PATIENT-CENTRIC HEALTHCARE INFORMATION MAINTENANCE - A system for facilitating patient centric healthcare information maintenance. For example, a health management software system may be operated to receive, organize, and use patient medical information. The health management software may comprise a database for storing, retrieving, organizing, displaying, and, generally, for managing a patient's health. In one exemplary embodiment, the health management software system is used in conjunction with a healthcare maintenance device, such as a blood glucose monitoring system. The blood glucose monitoring system may contain several database objects in the form of data records. Typically in a portable blood glucose monitor, each data record contains a time and a concentration data element, or a time-amount point. Similarly, an insulin pump, which is another exemplary embodiment of a healthcare maintenance device, may maintain data records with time and dosage information, or a time-dosage point. | 10-06-2011 |
| 20110244598 | Test Element Having Combined Control and Calibration Zone - A test element, for example in the form of an immunological test strip functioning according to the sandwich principle, for the fluorophoric detection of one or more analytes in a sample comprising an analyte detection zone and a combined control and calibration zone. The combined control and calibration zone include a fluorophore and binding partners for the specific binding of reagents labelled with a fluorophore. Furthermore, the invention concerns a method for calibrating an analyte-specific measurement signal, a method for determining the concentration of an analyte in a sample and the use of the test element for calibrating a signal generated in the analyte detection zone of a test element. | 10-06-2011 |
| 20110237979 | PRECISION DEPTH CONTROL LANCING TIP - A bodily fluid sampling device is operable to lance with a precise depth and express fluid from both fingertip and alternate sites. In one form, the device is operable to adjust the penetration depth of the lancet into the skin. The bodily fluid sampling device includes a lancet adapted to form an incision in skin. A skin contacting member has an orifice through which the lancet extends when lancing the skin. The orifice has a first opening size that is sized to flatten the skin around the lancet during lancing. The orifice has a second opening size that is larger than the first opening size after the incision is formed to express fluid from the incision. | 09-29-2011 |
| 20110230905 | TAPE TRANSPORT LANCE SAMPLER - A lancet-sampler system is configured to automatically remove a protective cover from a lancet and automatically unpack a test pad just prior to use. This minimizes the risk of injury and reduces the chance of cross-contamination between the lancet and the test pad. The lancet defines a capillary groove for drawing body fluid from the incision via capillary action and a sample transfer opening for collecting the fluid from the groove. A carrier tape is coupled to the lancet. The carrier tape includes a test pad for analyzing the fluid. The tape is folded around the test pad to form an airtight package. The test pad is located at a position to align with the sample transfer opening when the tape is unfolded. The protective cover covers a portion of the lancet, and when the tape is pulled, the protective cover is automatically pulled from the lancet. | 09-22-2011 |
| 20110230142 | METHOD AND SYSTEM FOR MULTI-DEVICE COMMUNICATION - A medical data system including a plurality of receivers configured to wirelessly receive medical data via a signal. | 09-22-2011 |
| 20110220715 | ANALYSIS SYSTEM FOR ANALYZING BIOLOGICAL SAMPLES, METHODS, AND COMPUTER PROGRAM PRODUCT THEREOF - An analysis system for analyzing biological samples, such as body fluids, methods implemented by the analysis system, and a computer program product for implementing the analysis system are disclosed. The system may include first and second lab devices, at least one of the lab devices may have a user identification component for identifying a user, a device identification component for identifying the lab device, and an interface component for sending a user identifier of the identified user and a device identifier of the lab device. The system may include a server computer having a server interface component for receiving the user identifier and the device identifier, and a processing component for determining a step of a workflow to be executed by the identified user, wherein the server interface component is operable to send a signal being indicative of a determined workflow to the lab device identified by the device identifier. | 09-15-2011 |
| 20110208027 | Methods And Systems For Providing Therapeutic Guidelines To A Person Having Diabetes - A method is disclosed for providing therapeutic guidelines to a person having diabetes. The method comprises measuring a blood glucose (bG) level of the person for two or more days, wherein at least one bG measurement is taken per day, and the at least one daily bG measurement corresponds to one or more daily events for the person; recording the measured bG levels in a computing device; determining, by the computing device, whether the recorded bG levels are below, within, or above one or more predetermined bG ranges; an automatically providing, by the computing device, therapeutic guidelines to the person, based on whether the recorded bG levels are below, within, or above the one or more predetermined bG ranges. | 08-25-2011 |
| 20110196213 | Display For Biological Values - Methods for providing an estimated or predicted biological values in a sectioned display to assess the relative impact of a set of variables include collecting biological measurements, grouping the biological measurements based on the set of variables, evaluating the biological measurements to determine grouped estimated biological values or grouped predicted biological values, and providing the grouped estimated biological values or grouped predicted biological values within a plurality of sections in the sectioned display, wherein the plurality of sections correspond to the set of variables. | 08-11-2011 |
| 20110194980 | Process For Hydrophilizing Surfaces Of Fluidic Components And Systems - A method for applying reactive films containing solids to microporous membranes is provided wherein the membrane is firstly moistened and the reactive film containing solids is applied to the membrane while it is still moist. Membranes produced in this manner can contain reactive films having a high proportion of film openers and can be used advantageously in diagnostic elements for detecting constituents and, in particular, large hydrophobic analytes in body fluids. | 08-11-2011 |
| 20110190701 | METHODS, SYSTEMS AND DEVICES FOR RECORDING DATA - Methods, systems and devices for recording data are described herein. In one embodiment a method for recording data for keeping a diary may include: storing primary data indicative of a measured blood glucose level and/or an administrated dose of insulin in a memory of an electronic diary device; receiving a spoken voice message with a microphone, wherein the spoken voice message is indicative of supplementary data directly related to the primary data; and storing the supplementary data in the memory of the electronic diary device, wherein the primary data is stored with a primary time stamp and the supplementary data is stored with the primary data, the primary time stamp or a supplementary time stamp. | 08-04-2011 |
| 20110189785 | PROCESSING UNITS AND METHODS FOR THE PROCESSING OF LIQUID SAMPLES - A microfluidic processing unit for the automated processing of liquid samples and method thereof are disclosed. In one embodiment, the unit comprises first and second main channels connected to a pump for generating a negative or positive pressure therein; a sample channel which supplies a liquid sample is connectable to a sample vessel containing the liquid sample, the sample channel communicates with the first main channel and is equipped with an on/off valve; one or more reagent channels for supplying one or more reagents, the reagent channels being connectable to reagent vessels containing reagents for reacting with the liquid samples, each of the reagent channels communicating with the first or second main channel and being equipped with an on/off valve; and a reaction chamber for reacting a sample and reagent, the reaction chamber being connected to the first and second main channels via at least one on/off valve. | 08-04-2011 |
| 20110189052 | System For The Analysis Of Liquid Samples - A system for the automated analysis of liquid samples having one or more processing units for reaction between the samples and one or more reagents to thereby obtain reaction products is disclosed. Disclosed also are a sample unit for supplying the samples to the one or more processing units; a reagent unit equipped with plural reagent vessels containing one or more reagents for mixing with the samples; a distribution unit for distributing fluids including the one or more reagents provided with plural distribution lines, at least some of which are connected to the reagent vessels and the one or more processing units; and at least one analytical unit for analyzing the samples based on the reaction products, in which the analytical unit may include at least one detector for detecting the reaction products. | 08-04-2011 |
| 20110186428 | ELECTRODE ARRANGEMENTS FOR BIOSENSORS - The present invention relates to a biosensor. The biosensor includes a support substrate, electrodes positioned on the support substrate, a spacer substrate positioned on the support substrate, and a cover positioned on the spacer substrate. The cover cooperates with the support substrate to define a capillary channel. The electrodes include at least one working electrode defining a working electrode area in the capillary channel. The working electrode is configured to minimize variation in the working electrode area in the capillary channel due to variations in the spacer substrate placement relative to the working electrode. | 08-04-2011 |
| 20110184267 | Methods And Systems For Processing Glucose Data Measured From A Person Having Diabetes - Methods and systems are disclosed for estimating a glucose level of a person having diabetes comprises. One method may comprise: receiving into a computing device a plurality of measured glucose results from a glucose sensor coupled to the person; using the computing device to analyze the plurality of measured glucose results with a probability analysis tool configured to determine a probability of glucose sensor accuracy based on the plurality of measured glucose results; and using the computing device to estimate a glucose level of the person with a recursive filter configured to estimate the glucose level based on the plurality of measured glucose results weighted with the probability of glucose sensor accuracy. | 07-28-2011 |
| 20110183432 | TEST ELEMENT FOR ANALYZING AN ANALYTE PRESENT IN A SAMPLE OF A BODY FLUID, ANALYSIS SYSTEM AND METHOD FOR CONTROLLING THE MOVEMENT OF A FLUID CONTAINED IN A CHANNEL OF A TEST ELEMENT - Embodiments disclosed herein include an analysis system for the analysis of a body fluid sample for an analyte contained therein, comprising a test element and an evaluation device having a measuring station for measuring a measuring variable on the measuring zone of the test element. Also included is a mounting to hold a test element, the test element having an airflow channel with two expansion sections and a narrow section located between these expansion sections. The expansion sections may have a cross-sectional area that increases in comparison to the narrow section in the direction away therefrom. A connection channel is located between the narrow section and the analysis function channel such that an air exchange connection is formed. The airflow channel is located in such a manner that a partial vacuum, which is generated using an airflow flowing through the airflow channel, acts on the analysis function channel. | 07-28-2011 |
| 20110182785 | Flat Pop-Up Primary Container And Methods of Manufacturing And Utilization Thereof - A test strip container with a pop-up design which provides easy removal of test strips, and methods of manufacturing and utilization thereof are disclosed. The test strip container comprises a base, a lid, and an elevating platform which translates in a vertical direction upon opening of the test strip container. The test strips are arranged within the base such that they face radially inward and rest upon the elevating platform. Translation of the elevating platform causes the test strips resting upon the platform to translate upward in a perpendicular manner, such that they may be easily removed by test strip users. | 07-28-2011 |
| 20110182774 | Plastic Injection-Moulded Part With Embedded Component - A method for producing a plastic injection-moulded part having an insert made of a material different from the plastic material is provided, the method comprising the steps of: (a) introducing and positioning the insert in a cavity of an injection mould; (b) setting the clamping force of the injection mould on a clamping mechanism to a maximum force predetermined by the material of the insert; and (c) seamlessly encapsulating the insert with the plastic material of the plastic injection-moulded part inside the injection mould, wherein the encapsulating is seamless or complete. | 07-28-2011 |
| 20110178820 | Status Reporting Of A Structured Collection Procedure - Embodiments related to a system and method managing the implementation, execution, data collection, data analysis and status reporting of a structured collection procedure running on a portable, hand-held collection device are disclosed. The collection device performing the structured collection procedure has program instructions that when executed by a processor cause the processor to initiate automatically a schedule of events of the structured collection procedure upon one or more entry criteria being met at some unknown time, store in memory patient data collected in accordance to the schedule of events, end automatically the structured collection procedure upon one or more exit criteria being met at some unknown time. Status reporting can be provided throughout the execution of the collection procedure. | 07-21-2011 |
| 20110177605 | On-Board Control for Analytical Elements - The invention concerns a reagent system for the so-called on-board control of analytical elements, in particular test strips, containing an organic N-oxide or a nitroso compound. The invention also concerns analytical elements containing a reagent system for a detection reaction and a reagent system for an on-board control. Furthermore, the invention concerns a method for checking analytical elements in which a reagent system for an on-board control is examined optically or electrochemically with the aid of a measuring instrument for changes which could indicate a stress of the analytical element. | 07-21-2011 |
| 20110177514 | INTEGRATED INSTRUMENT PERFORMING SYNTHESIS AND AMPLIFICATION, AND A SYSTEM AND METHOD THEREOF - An integrated instrument for oligonucleotide synthesis and PCR, and a system and method thereof are disclosed. The integrated instrument is basically composed of two independent modules. The first module is a unit for chemical de novo synthesis of oligonucleotides such as oligonucleotide primers and/or oligonucleotide hybridization probes. The second module is a unit for performing an analytical polymerase chain reaction amplification in real time, i.e. a qPCR. The two modules are operatively linked to each other in such a way that a user can load a nucleic sample to be analyzed into the integrated instrument and perform a PCR reaction by programming the instrument without a previous external synthesis of oligonucleotide amplification primers. | 07-21-2011 |
| 20110174644 | TEST STRIP CONTAINER WITH STRIP RETAINER AND METHODS OF MANUFACTURING AND UTILIZATION THEREOF - A test strip container with an insert comprising a channel and a retaining member and methods of manufacturing and utilization thereof are disclosed. The container includes a housing, an insert, a lid, and at least one retaining member in at least one channel. The at least one retaining member releasably retains a plurality of test strips in the at least one channel. | 07-21-2011 |
| 20110173024 | INDIVIDUALIZATION OF MEDICAL ADJUVANTS - A method for upgrading a medical device for the treatment of diabetes in the home-monitoring field includes the steps of providing consumables in a housing with a type-specific identification code for use in a medical device, storing the identification code in combination with a user identification and determining a user status, offering a selection according to the user status of at least one configuration of a supplemental module for the medical device, and generating a delivery order for a supplemental module based on the selection made by the user. | 07-14-2011 |
| 20110154237 | METHODS, SYSTEMS AND COMPUTER READABLE MEDIA FOR MODIFYING PARAMETERS OF A CONFIGURATION FILE - Disclosed is a method of configuring a medical device through utilization of a computing device that includes a user interface, a processor and memory. The method includes the steps of determining whether a configuration file contains a focal modified parameter, displaying the focal modified parameter, prompting a manual re-entry of the displayed focal modified parameter, receiving through the user interface the manual re-entry of the displayed focal modified parameter, and utilizing the processor to automatically determine whether the manual re-entry of the displayed focal modified parameter matches the displayed focal modified parameter. | 06-23-2011 |
| 20110152769 | METHODS AND SYSTEMS FOR ADJUSTING AN INSULIN DELIVERY PROFILE OF AN INSULIN PUMP - Systems and methods are disclosed for adjusting the delivery times of an insulin delivery profile of an insulin pump, wherein the insulin pump is operable to automatically deliver insulin to a person having diabetes based on an operating time of the internal clock and a delivery time of an insulin delivery profile. The method may comprise receiving a local time zone time from an external local clock, determining whether the operating time of the internal clock differs from the local time zone time by at least a first predetermined amount of time, requesting the person provide a time adjustment value when the operating time of the internal clock differs from the local time zone time by at least the first predetermined amount of time, receiving the time adjustment value from the person, and adjusting the delivery times of the insulin delivery profile based on the time adjustment value when received. | 06-23-2011 |
| 20110152757 | MEDICINAL FLUID DELIVERY SYSTEMS AND METHODS FOR PRIMING THE SAME - Medicinal fluid delivery systems and methods for priming the same are disclosed. The systems may be configured to measure an electro-transmissive quality of a medicinal fluid when: medicinal fluid is dispensed into a fluid delivery path, a proximal end of the fluid delivery path is in contact with a first electrode, and the distal end of the fluid delivery path is in contact with a second electrode. Methods for priming medicinal fluid delivery systems may include dispensing a medicinal fluid through a fluid delivery path, sensing an electro-transmissive quality of the medicinal fluid, and determining that the fluid delivery path is full based on the electro-transmissive quality. | 06-23-2011 |
| 20110152656 | Collection Device With Selective Display of Test Results, Method And Computer Program Product Thereof - A collection device with a selective display of test results and method thereof are disclosed. A structured collection procedure defining data collection times and the associated context of the collection also defines what information regarding the results of the collection may be viewable by a user performing the structured collection procedure on the device. In this manner, the patient can be monitored according to the structured collection procedure while preventing the patient from modifying his or her behavior based on collection results. | 06-23-2011 |
| 20110152655 | SYSTEMS AND APPARATUSES FOR TESTING BLOOD GLUCOSE MEASUREMENT ENGINES - A system for testing a blood glucose measurement engine includes a host device emulator having a measurement engine port communicatively coupled to a communications port and electrically coupled to a power supply. A diagnostic computer may be communicatively coupled to the communications port of the host device emulator. The diagnostic computer may include a processor and a memory having computer readable and executable instructions. When the blood glucose measurement engine is communicatively coupled to the measurement engine port, the host device emulator simulates connection to a host device by facilitating the communication of signals between the diagnostic computer and the blood glucose measurement engine. The processor executes the computer readable and executable instructions to: transmit control signals and diagnostic signals to the measurement engine, receive and analyze data signals transmitted from the measurement engine, and monitor a glucose measurement process performed by the measurement engine. | 06-23-2011 |
| 20110151571 | MEMORY APPARATUS FOR MULTIUSE ANALYTE TEST ELEMENT SYSTEMS, AND KITS, SYSTEMS, COMBINATIONS AND METHODS RELATING TO SAME - One embodiment includes a memory unit for use in connection with a plurality of fluid sample test elements, wherein the memory unit comprises a plurality of memory portions. In one aspect of the embodiment, the memory unit comprises at least one memory portion configured to communicate calibration and expiration information relating to a lot of test elements, to a meter operably connectable with such test elements, and at least one other memory portion configured for storage and communication of data, such as measurement results, relating to the use of the test elements in analyzing a fluid sample. Further embodiments include apparatuses, systems, methods, kits and combinations of test elements and memory units. | 06-23-2011 |
| 20110147244 | EASY STRIP ACCESS PRIMARY CONTAINER AND METHODS OF MANUFACTURING AND UTILIZATION THEREOF - Embodiments of the present invention relate to a test strip container which provides easy access to test strips. The test strip container includes a lower housing, an upper housing, and a retaining member configured to releasably retain the test strips in a nested configuration. The nested configuration of the test strip container provides easy access to test strips by arranging the test strips so that they extend radially outward from the retaining member. The radial arrangement of the test strips operates to separate the test strips so that test strip users may easily select a single test strip from a plurality of test strips. Alternatively, the test strip container includes a lower housing, an upper housing, and a retaining member configured to releasably retain the test strips in a longitudinal configuration. | 06-23-2011 |
| 20110145747 | Structured Tailoring - Embodiments related to a self-administered, behavior modification program facilitated through a structured tailoring method and system thereof which accelerates and enhances the internalization process of the individual, and which provides help when the individual begins to fail in adhering or continuing with the behavior modification are disclosed. Program instructions that when executed by a processor causes a processor to initiate automatically a schedule of events of a structured tailoring procedure upon entry criteria being met at some unknown time, provide intervention according to the intervention preferences when the adherence criteria for one of the events has not been met, and end automatically the structured collection procedure upon exit criteria being met at some unknown time. | 06-16-2011 |
| 20110136109 | System And Method For Cycling Liquid Samples Through A Series Of Temperature Excursions - A system and method for cycling liquid samples through a series of temperature excursions are disclosed. Provided are open-top reaction vessels for containing the samples, which may be enclosed by one or more covers. A temperature-controlled block for generating or adsorbing heat is coupled thermally to the reaction vessels. A detection arrangement is disposed in an emission beam path to detect radiation emitted from the samples through the covers. A heating arrangement for generating heat includes a heating element that is both disposed between the reaction vessels and the detection arrangement and coupled thermally to the covers. The heating element includes an optically transparent substrate provided with one or more opaque heating lines, the heating lines being disposed in the emission beam path in a manner to obtain a predetermined minimum optical transmission of the heating element. A controller, set up to control cycling of the samples, is provided. | 06-09-2011 |
| 20110129914 | THERMOCYCLING OF A BLOCK COMPRISING MULTIPLE SAMPLE - The present invention relates to the field of high throughput analysis of samples. In particular, the present invention is directed to a device, a system and a method for simultaneous tempering of multiple samples. More particular, the invention relates to the simultaneous thermocycling of multiple samples to perform PCR in a microtiter plate format. | 06-02-2011 |
| 20110127292 | System And Method For Dispensing Fluids - A system for dispensing one or more fluids into wells of a target multi-well plate, a holder and a method thereof are disclosed. The system provides the holder which holds the multi-well plate in a predefined holding position, the plate having a well region provided with wells for accommodating the fluids and an edge region surrounding the well region. The holder includes: a contact area which contacts the edge region to form a sealing zone which air-tightly seals a void formed between the holder and the plate; a supporting face which supports the well region in a planar condition; and a duct which connects to a pump to generate a negative pressure in the void so as to draw the well region onto the supporting face. | 06-02-2011 |
| 20110127175 | TEST STRIP CONTAINER WITH EXPANDABLE INSERT AND METHODS OF MANUFACTURING AND UTILIZATION THEREOF - A test strip container with an expandable insert, and methods of manufacturing and utilization thereof are disclosed. The container includes a housing defining a cavity, a lid, and a compressible insert removably mounted in the cavity. The compressible insert is expandable to retain a plurality of test strips in the cavity and to protect the test strips from environmental degradation. | 06-02-2011 |
| 20110124996 | DIABETES HEALTH MANAGEMENT SYSTEMS AND METHODS - Diabetes health management systems for use in portable devices having and methods thereof having a user interface, a processor, a memory, and a communication circuit are disclosed. In one embodiment, a diabetes health management system has program code further including a communications module, a data module, a therapy module, and an analysis module. The communications module wirelessly couples the portable device to a plurality of user devices. The data module receives and stores into the memory blood glucose measurement values, insulin dosage data, and health data entries. The therapy module determines a therapy advice message based at least in part on the received blood glucose measurement values, the received insulin dosage data, and displays the therapy advice message on the user interface. The analysis module displays on the user interface a graphical representation of selected blood glucose measurement values, selected insulin dosage data, selected health data entries, or combinations thereof. | 05-26-2011 |
| 20110124128 | Centrifugal Force Based Microfluidic System And Method For The Automated Analysis of Samples - Centrifugal force based microfluidic systems for the automated analysis of fluids involving the use of magnetically responsive particles and methods thereof are disclosed. A magnet is fixed to a supporting device of the system in correspondence to a retention zone of the system so as to rotate therewith and to generate a magnetic field which magnetically manipulates the magnetically responsive particles contained in a reaction chamber of the system. | 05-26-2011 |
| 20110118578 | HYPOGLYCEMIC TREATMENT METHODS AND SYSTEMS - A system for treating hypoglycemia includes a continuous blood glucose monitor that monitors blood glucose levels of a patient on a continuous basis over a period of time. An alarm and injector apparatus is configured to be worn by the patient and includes a glucagon delivery mechanism for automatically delivering glucagon to the patient if a hypoglycemic condition is detected using the continuous blood glucose monitor. | 05-19-2011 |
| 20110111506 | System And Method For Pipetting Of Fluids, Method For Calibrating The System - A system and a method for the automated pipetting of fluids are disclosed as well as a method for calibrating the system. A channel pump having at least one tip-sided port connected to a pipetting tip by a tip-sided pump conduit for generating a positive or negative pressure in the pipetting tip, and at least one reservoir-sided port connected to a system fluid reservoir by a reservoir-sided pump conduit is provided. The channel pump when operated at a nominal flow rate exhibits a fluid backflow caused by a pressure difference in the tip- and reservoir-sided pump conduits which results in an effective flow rate compared to the nominal flow rate. Such a pressure difference can be used to determine an extended pipetting period which extends a pipetting period of the channel pump operating at the nominal flow rate, and to calibrate the system. | 05-12-2011 |
| 20110110063 | Robust Consumer Electronic Device - A method includes providing a molded elastomeric mat having an input protrusion, an output device receiving surface including an output device contact, and a battery receiving indentation including a power supply contact. The method further includes insert molding an output conductive path into the elastomeric mat, the output conductive path electrically coupling a circuit carrier output contact to an output device contact, and insert molding a power supply conductive path into the elastomeric mat, the power supply conductive path electrically coupling a circuit carrier power contact to the power supply contact. The method includes interfacing the elastomeric mat with a circuit carrier, aligning the input protrusion with a circuit carrier input contact, interfacing a display device with the output device receiving surface, electrically connecting the display device with the output device contact, and positioning the elastomeric mat into a housing. | 05-12-2011 |
| 20110093510 | METHODS AND SYSTEMS FOR SERIALLY TRANSMITTING RECORDS IN XML FORMAT - A portable electronic medical device and method for serially transmitting one or more records from the portable electronic medical device are disclosed. The portable electronic medical device includes a processor and memory for storing the one or more records, each record having one or more data entries. An XML (Extensible Markup Language) template may be parsed by the processor, wherein the XML template has one or more XML elements associated with the one or more data entries. The one or more records may be read as well as the XML elements appended to the associated data entries of each record by the processor such that the appended data entries are in XML format. The processor may then serially transmit the appended data entries of each record. | 04-21-2011 |
| 20110092788 | Systems And Methods For Providing Guidance In Administration Of A Medicine - A method of providing guidance using a portable hand-held electronic device in administration of a medicine by a patient is provided. The method includes acquiring image data of a first container of a first medicine prescribed to the patient and acquiring image data of a second container of a second medicine prescribed to the patient. The second container is different visually from the first container. The image data of the first container and the second container is stored in memory of the electronic device. On the portable hand-held electronic device, an instruction is processed to administer at least one of the first medicine and the second medicine to the patient. The stored image data is retrieved from memory corresponding to the at least one of the first medicine and the second medicine to be administered in the instruction. The retrieved image data is displayed on a display of the electronic device. | 04-21-2011 |
| 20110091914 | Immunological Test Element with Improved Control Zone - The invention concerns a test element for carrying out an immunological sandwich test for determining an analyte from a liquid sample containing a reagent zone or conjugate zone which contains a conjugate of an analyte binding partner and a label which can be detected directly or indirectly by visual, optical or electrochemical means (e.g., an enzyme, fluorescent or direct label, etc.) wherein the conjugate can be dissolved by the liquid sample, a detection zone which contains a permanently immobilized (i.e., which cannot be detached by the liquid sample) binding partner for the analyte or for complexes containing the analyte; and a control zone which contains a permanently immobilized binding partner for the conjugate of analyte binding partner and label characterized in that the control zone additionally contains one or more permanently immobilized binding partner(s) for the analyte or for complexes containing the analyte. | 04-21-2011 |
| 20110079523 | Gas Sensor With a Microporous Electrolyte Layer - The present invention relates to electrochemical sensors for determining gaseous analytes in an aqueous measuring medium, to a process for producing such sensors, and to a process for determining gaseous analytes dissolved in an aqueous measuring medium using the electrochemical sensors. The electrolyte layer of the sensors comprises at least one particulate material and at least one binder which together form a porous, non-swellable framework structure, wherein the pores in this framework structure are configured to absorb a liquid electrolyte or contain the liquid electrolyte. | 04-07-2011 |
| 20110066805 | Process For The Management Of Data Of Analysis Devices, Analysis Device And System Comprising Analysis Devices - A process for the management of data of an analysis device, which data serve for the operation of a further analysis device which is designed so as to be equivalent to the first analysis device, is disclosed. The analysis device newly creates or modifies data on an internal memory medium of the analysis device and the first analysis device, during its operation, continuously stores the newly created or modified data in a redundant manner in a non-volatile removable storage medium, with the removable storage medium being independent of the internal memory medium. | 03-17-2011 |
| 20110056951 | STORAGE CONTAINERS FOR TEST ELEMENTS - A container includes an external housing having a sidewall extending between a first end and a second end, and an internal chamber extending between the first and second ends and surrounded by the sidewall. The container includes a sleeve member in the internal chamber. The sleeve member may include corrugated desiccant in communication with the internal chamber, or a porous member to maintain desiccant between the internal chamber and the sidewall. The container may also include at least one component in the internal chamber, such as a test element, for use with a biosensor. Other embodiments include unique methods, systems, kits, assemblies, equipment, and/or apparatus which are related to containers including one or more desiccants or desiccant materials. | 03-10-2011 |
| 20110034786 | PORTABLE HANDHELD MEDICAL DIAGNOSTIC DEVICES - A portable handheld medical diagnostic device includes a front housing and a rear housing opposite the front housing. The front housing and the rear housing form a protective enclosure. A main circuit board is located in the protective enclosure. The main circuit board includes a controller facilitating a physiologic measurement. A display device is connected to the main circuit board that displays information related to the physiologic measurement. A frame is located in the protective enclosure that carries the display device and locates the display device adjacent the front housing such that the display device can be viewed from outside the protective enclosure. The frame includes a strip port formed integrally therewith that is accessible from outside the protective enclosure. | 02-10-2011 |
| 20110030803 | Sample Preparation Dosing Unit - A sample preparation dosing unit for liquid dosing is provided comprising an inlet port and an outlet port fluidically coupling the sample preparation dosing unit to a supply and target, respectively; a pump, fluidically arranged between the inlet port and the outlet port; an outlet flow restrictor with an outlet flow resistance, fluidically arranged between a pump outlet and outlet port; and a control arrangement with a branch, a control valve, and a control flow restrictor with a control flow resistance. The branch divides the flow at the pump outlet into an outlet flow through the outlet flow restrictor and into a control flow through the control flow restrictor. The control flow downstream of the control flow restrictor is fed, depending on the state of the control valve, either into the outlet port thereby merging with the outlet flow downstream of the outlet flow restrictor, or into a bypass conduit. | 02-10-2011 |
| 20110015511 | SYSTEMS AND METHODS FOR OPTIMIZING INSULIN DOSAGE - Embodiments of a testing method suitable for diabetic persons to optimize their administered insulin dosage comprise collecting one or more sampling sets of biomarker data, wherein each sampling set comprises a sufficient plurality of non-adverse sampling instances and wherein each sampling instance comprises an acceptable biomarker reading at a single point in time recorded upon compliance with adherence criteria, determining a biomarker sampling parameter from each sampling set, comparing the biomarker sampling parameter to a target biomarker range, calculating an insulin adjustment parameter associated with the biomarker sampling parameter if the biomarker sampling parameter falls outside the target biomarker range, adjusting the insulin dosage by the insulin adjustment parameter if the biomarker sampling parameter falls outside the target biomarker range and if the insulin dosage does not exceed maximum dosage, and exiting the testing method if the adjusted insulin dosage is optimized. The insulin dosage is optimized when one or more biomarker sampling parameters fall within a target biomarker range. | 01-20-2011 |
| 20100331652 | MODULAR DIABETES MANAGEMENT SYSTEMS - In one embodiment, a modular diabetes management system includes a portable, stand-alone blood glucose meter and a portable docking device that includes an internal receptacle sized and structured to receive and house the blood glucose meter. The docking device is generally operable to interface with the blood glucose meter and perform various diabetes management functions. For example, the docking device may be operable to analyze blood glucose measurement data stored on the blood glucose meter, configure the blood glucose meter, and/or interact with an insulin delivery device, just to name a few possibilities. Other embodiments include unique methods, systems, kits, assemblies, equipment, and/or apparatus which are related to the management of diabetes. | 12-30-2010 |
| 20100331651 | BLOOD GLUCOSE MANAGEMENT AND INTERFACE SYSTEMS AND METHODS - A blood glucose management device is operable to seamlessly provide a sequence of at least two displays of data relating to one or more blood glucose measurements to a user, upon minimal user interaction, with the blood glucose management device. | 12-30-2010 |
| 20100331650 | EPISODIC BLOOD GLUCOSE MONITORING SYSTEM WITH AN INTERACTIVE GRAPHICAL USER INTERFACE AND METHODS THEREOF - A blood glucose monitoring system with a graphical user interface (GUI) and methods of controlling the system and performing episodic blood glucose testing using the GUI are disclosed. The system can comprise the GUI, an output display for displaying the GUI, user interfaces, a memory and a processor. An episodic blood glucose testing protocol can be programmed into the processor using the user interfaces and automatically saved into memory. A user can be alerted to test blood glucose levels based on the inputted testing protocol by the display of an alert icon on the GUI. Blood glucose level results can be received, displayed on the GUI along with a range icon and automatically saved into memory. Statistics of the saved blood glucose results can be calculated by the processor and saved into memory. The statistics can be retrieved for display on the GUI when prompted by the user. | 12-30-2010 |
| 20100331645 | METHODS AND SYSTEMS FOR WIRELESS COMMUNICATION BETWEEN A BLOOD GLUCOSE METER AND A PORTABLE COMMUNICATION DEVICE - A blood glucose measuring system which comprises a blood glucose (bG) meter and a portable communication device (PCD) and methods thereof are disclosed. The blood glucose meter comprises a measurement module and a wireless module, wherein the measurement module is operable to measure the blood glucose level of a blood sample, the wireless module is an embeddable module and communicates to the measurement module via a serial interface, and the wireless module is operable to wirelessly communicate to the portable communication device. The portable communication device is operable to wirelessly receive information from the blood glucose meter related to the blood glucose measurement. | 12-30-2010 |
| 20100331627 | ADHERENCE INDICATION TOOL FOR CHRONIC DISEASE MANAGEMENT AND METHOD THEREOF - An adherence indication tool for chronic disease self-management and method thereof for measuring adherence or compliance to following or achieving prescribed therapy steps to achieve stated target goals for improved chronic disease self-management are disclosed. | 12-30-2010 |
| 20100330705 | Immunological Test Element with Improved Control Zone - The invention concerns a test element for carrying out an immunological sandwich test for determining an analyte from a liquid sample containing a reagent zone or conjugate zone which contains a conjugate of an analyte binding partner and a label which can be detected directly or indirectly by visual, optical or electrochemical means (e.g., an enzyme, fluorescent or direct label, etc.) wherein the conjugate can be dissolved by the liquid sample, a detection zone which contains a permanently immobilized (i.e., which cannot be detached by the liquid sample) binding partner for the analyte or for complexes containing the analyte; and a control zone which contains a permanently immobilized binding partner for the conjugate of analyte binding partner and label characterized in that the control zone additionally contains one or more permanently immobilized binding partner(s) for the analyte or for complexes containing the analyte. | 12-30-2010 |
| 20100330598 | METHOD, SYSTEM, AND COMPUTER PROGRAM PRODUCT FOR PROVIDING BOTH AN ESTIMATED TRUE MEAN BLOOD GLUCOSE VALUE AND ESTIMATED GLYCATED HEMOGLOBIN (HbA1C) VALUE FROM STRUCTURED SPOT MEASUREMENTS OF BLOOD GLUCOSE - A method and system for providing both an estimated true mean blood glucose value and estimated glycated hemoglobin (HbA1C) value from spot blood glucose (bG) measurements are disclosed. The bG measurements and associated context of the bG measurement are collected at daily times specified by a structured sampling schema, and the collected bG measurements are weighted based on the associated context. The estimated true mean bG value and the estimate HbA1C value are then determined from the weighted measurements of the collected bG measurements. A computer program for implementing the method for providing both an estimated true mean blood glucose value and estimated glycated hemoglobin (HbA1C) value from spot blood glucose (bG) measurements is also disclosed. | 12-30-2010 |
| 20100324932 | METHODS AND SYSTEMS FOR ADVISING PEOPLE WITH DIABETES - A method and system for advising a person with diabetes to perform a task based on the recommended therapy are disclosed. A library of one or more tasks is established, wherein each task in the library is related to a therapy recommended to the person with diabetes. Personal and real-time data related to the person's diabetic condition are recorded such that advice provided to the person to perform a task from the library is based on the recorded personal and real-time data. In this manner, the embodiments of the present invention simplify the ability of a person with diabetes to follow a recommended therapy. | 12-23-2010 |
| 20100323431 | BI-STABLE DISPLAY FAIL SAFES AND DEVICES INCORPORATING THE SAME - A control circuit and method for controlling a bi-stable display having bi-stable segments each capable of transitioning between an on state and an off state via application of a voltage are disclosed. The voltage is provided to a display driver from a charge pump, and supplied to individual ones of the bi-stable segments via outputs from the display driver in accordance with display instructions provided by a system controller. Both a bi-stable segment voltage level of at least one of the outputs of the display driver and a charge pump voltage level of the voltage are detected and compared to a valid bi-stable segment voltage level and a valid charge pump voltage level, respectively. A malfunction signal may be provided to the system controller if either of the detected voltage levels is not valid. The control circuit is useful in an electronic device such as, for example, a blood glucose measuring device. | 12-23-2010 |
| 20100317951 | PORTABLE HANDHELD MEDICAL DIAGNOSTIC DEVICES WITH COLOR-CHANGING INDICATOR - A portable handheld medical diagnostic device includes a housing forming a protective enclosure. A main circuit board is located in the protective enclosure. The main circuit board includes a controller facilitating a physiologic measurement. A display device is connected to the main circuit board that displays information related to the physiologic measurement. An electronic skin is on the housing. The electronic skin comprises a liquid crystal material and is configured to display a color. | 12-16-2010 |
| 20100317950 | DEVICE, METHOD, AND GRAPHICAL USER INTERFACE FOR SEARCHING, FILTERING AND DISPLAYING EVENT-ALIGNED INFORMATION SETS RELATED TO DIABETES - A device, method, and graphical user interface for displaying diabetes related information sets aligned by the occurrence of a particular event are disclosed. After receiving a request for an event-aligned display of diabetes related information based on an event, a search for a plurality of tagged occurrences of the event and retrieval of an information set for each of the plurality of tagged occurrences is provided. Each information set may include diabetes related information chronologically related to the tagged occurrence. The retrieved information sets is displayed on a display, wherein the retrieved information sets are shown on the display aligned by their tagged occurrences such that all diabetes related information is positioned relative the event based on its chronological relationship with the event. | 12-16-2010 |
| 20100307916 | TEMPERATURE ESTIMATIONS IN A BLOOD GLUCOSE MEASURING DEVICE - Methods of estimating the temperature of a reaction site on a measurement strip in a blood glucose measuring devices are provided. In one embodiment, a method includes determining an activation initiation time, an activation duration time, a thermal magnitude and a temperature elevation for heat generating components within a device. The temperature elevation for each of the heat generating components is determined at least in part by an impulse response matrix [X | 12-09-2010 |
| 20100287477 | Analysis System For Analyzing Biological Samples, Data Processing Method And Computer Program Product - Embodiments related to analysis system for analyzing biological samples, a data processing method and a computer program product are disclosed. An analyzer is coupled to an control computer and has a control application program which receives control data, sends analytical data, and generates a host screen image. A remote computer is coupled to the control computer, and provides a data manager application program which sends the control data to the control computer, receives the analytical data, and generates a first window. A remote application program interoperates with a host application program which generates a second window containing a duplicate of the host screen image. A user interface program displays a first display window and a second display window, the first display window being one of the first and second windows and the second display window containing a screen shot of the other one of the first and second windows. | 11-11-2010 |
| 20100286561 | TEST STRIP DEVICE AND METHOD FOR ANALYZING A BODY FLUID - The invention concerns a test tape device for analyzing a body fluid having a carrier tape ( | 11-11-2010 |
| 20100277727 | Method for Detecting Contaminants - A method for the detection of contaminants in an optical measuring cuvette of a spectrophotometer, typically an oximeter for determining hemoglobin derivatives, is provided, in which measuring cuvette, in addition to at least one sample measurement to obtain a sample spectrum I(λ), at least one reference measurement is performed using a reference liquid to obtain a reference spectrum I | 11-04-2010 |
| 20100233036 | REAGENT CONTAINER SYSTEM - A reagent container system for a reagent analyzer, in particular an automatic reagent analyzer, is disclosed. The system includes a first reagent container cassette provided with a first set of openings each being capable of containing a reagent therein, and a second reagent container cassette provided with a second set of openings each being capable of containing a reagent therein. The system provides the first and second reagent container cassettes at least in a storage configuration in which the container cassettes are joined together such that a longitudinal side of the first reagent container cassette is facing a longitudinal side of the second reagent container cassette. Wherein, by relative displacement, the first and second reagent container cassettes are displaceable between the storage configuration and a use configuration in which a transverse side of the first reagent container cassette is facing a transverse side of the second reagent container cassette. | 09-16-2010 |
| 20100222799 | JOINING FOILS WITH LASER FOR STERILE LANCETS - A process for manufacturing packaged lancets, comprising the steps:
| 09-02-2010 |
| 20100222704 | METHODS AND APPARATUS FOR SAMPLING AND ANALYZING BODY FLUID - A sampling device for sampling body fluid includes a lancet for making an incision, a capillary tube for drawing-up body fluid from the incision, and a test strip affixed to an upper end of the capillary tube for receiving the fluid. An absorbent pad can be disposed between the test strip and capillary tube for spreading-out the fluid being transferred to the test strip. An on-site analyzer such as an optical analyzer and/or an electrochemical analyzer can be mounted in the device for analyzing the fluid. Alternatively, a test strip can be slid through a slot formed in the bottom end of the device so that by passing the device against the skin after an incision has been formed, the test strip will directly contact body fluid emanating from the incision. | 09-02-2010 |
| 20100222656 | METHODS AND APPARATUS FOR SAMPLING AND ANALYZING BODY FLUID - A sampling device for sampling body fluid includes a lancet for making an incision, a capillary tube for drawing-up body fluid from the incision, and a test strip affixed to an upper end of the capillary tube for receiving the fluid. An absorbent pad can be disposed between the test strip and capillary tube for spreading-out the fluid being transferred to the test strip. An on-site analyzer such as an optical analyzer and/or an electrochemical analyzer can be mounted in the device for analyzing the fluid. Alternatively, a test strip can be slid through a slot formed in the bottom end of the device so that by passing the device against the skin after an incision has been formed, the test strip will directly contact body fluid emanating from the incision. | 09-02-2010 |
| 20100218132 | MANAGEMENT METHOD AND SYSTEM FOR IMPLEMENTATION, EXECUTION, DATA COLLECTION, AND DATA ANALYSIS OF A STRUCTURED COLLECTION PROCEDURE WHICH RUNS ON A COLLECTION DEVICE - Embodiments related to a system and method managing the implementation, execution, data collection, and data analysis of a structured collection procedure running on a portable, hand-held collection device are disclosed. The collection device performing the structured collection procedure has program instructions that when executed by a processor causes the processor to initiate automatically a schedule of events of the structured collection procedure upon one or more entry criterions being met at some unknown time, store in memory patient data collected in accordance to the schedule of events, end automatically the structured collection procedure upon one or more exit criterions being met at some unknown time, and mark/indicate the structured collection procedure as completed if no exception occurred during performance of an event in the schedule of events. | 08-26-2010 |
| 20100212675 | STRUCTURED TESTING METHOD FOR DIAGNOSTIC OR THERAPY SUPPORT OF A PATIENT WITH A CHRONIC DISEASE AND DEVICES THEREOF - A structured testing method for diagnostic or therapy support of a patient with a chronic disease and devices thereof are disclosed which implement a structured collection procedure based on a medical use case and/or question which provides at least one or more parameters defining entry criterion, a schedule of events, adherence criterion, and exit criterion. The entry criterion establish conditions needed to be met prior to obtaining biomarker data from the patient. Each event can include one or more of a performance time, patient guidance to perform the event, a request for information from the patient a request for patient action, and a request for collection of biomarker data from the patient. The adherence criterion can be used to assess whether an event performed is acceptable to addressing the medical use case and/or question, and the exit criterion establishes conditions needed to be met prior to exiting the collection procedure. | 08-26-2010 |
| 20100198107 | INTEGRATED BLOOD GLUCOSE METER AND LANCING DEVICE - An integrated medical testing device includes a testing meter and lancing device, the meter having a housing, a display, a test element opening, a firing mechanism and a navigation mechanism integrated with a lancing device. The lancing device is at least partially located in the housing and includes a tip having an opening through which a lancet extends upon firing. Various mechanisms can be used to extend the tip from the housing and to prime and fire the lancing device. The lancing device can accommodate a single lancet or a cartridge having multiple lancets. If a cartridge is used, various mechanisms can be utilized to position an unused lancet for firing after a test has been conducted. The relative locations of the lancing device and test element opening are such that the integrated meter and lancing device can be used with a test element inserted in the test element opening. The integrated meter and lancing device can include status indicators that reflect the state of the lancing device. | 08-05-2010 |
| 20100188244 | Orientation Identification Label, Reagent Container Carrier Structure, Analyzer Device And Reader Module - A reagent container carrier structure for holding at least one reagent container, wherein the carrier structure has thereon an RFID assembly and an optically detectable definition pattern defining an orientation of the carrier structure, is disclosed. The reagent container carrier structure may have an orientation identification label that has a front surface and a back surface, and further include an RFID assembly positioned on the back surface, and an optically detectable definition pattern defining an orientation of the label on the front surface. A reader module for reading RFID data in combination with optically detectable data defining an orientation of a respective label is also disclosed. | 07-29-2010 |
| 20100174211 | BODY FLUID LANCING, ACQUIRING, AND TESTING CARTRIDGE DESIGN - A disposable device for analyzing body fluid especially for blood sugar tests includes a container which can be inserted into a measuring apparatus, a sampling member provided in the container to pierce skin of a body part and sample body fluid, and a test member for receiving body fluid obtained by the skin-piercing. In one form, the test member is fixed in a retaining chamber of the container, and the sampling member is configured in the same retaining chamber such that it is separated at a distance from the test member in an initial state and is in contact with the test member to transfer body fluid in a transfer state after the skin-piercing. | 07-08-2010 |
| 20100161267 | Device and Method for Automatic Calibration Verification of an Analyzer - A method and a device for carrying out calibration verification (CV process) of an analyzer for determining different measurement parameters in body fluids is provided. The device according to the invention comprises the following components: a cartridge with a plurality of containers, which can be connected to an intake system of an analyzer, each of which contains a measurement fluid with known measurement parameter values; a storage unit assigned to the cartridge for storing the measurement parameter values of the measurement fluids and data relevant for the CV process of the analyzer to be verified; a docking or intake area at or in the analyzer for receiving the cartridge with a data path for reading the storage unit; an evaluation unit typically housed in the analyzer for evaluating the values measured by the analyzer; and an output unit for printing an evaluation protocol. | 06-24-2010 |
| 20100160757 | DEVICE AND METHOD FOR ASSESSING BLOOD GLUCOSE CONTROL - A blood glucose and lifestyle tracking apparatus is disclosed. The blood glucose and lifestyle tracking apparatus provides a method for recording both blood glucose values for fasting, postprandial, and preprandial time periods and lifestyle factors. | 06-24-2010 |
| 20100159500 | Method for determining the haemolysis of a blood sample and device - The invention relates to a method for determining the haemolysis of a blood sample during which the haemolysis progress is determined, wherein the method comprises the steps of irradiating measuring light which is radiated from a measuring light source on the blood sample during haemolysis; detecting measuring light values at several measuring points of time for measuring light transmitted through and/or reflected by the blood sample by a detector device; comparing several of the measuring light values for different measuring points of time and determining a measure for the haemolysis progress by an evaluation device by forming a time-dependent course for the measuring light values from the detected measuring light values, and determining for the time-dependent course at least section-wise a gradient in an assigned measuring curve as a comparative measure for the comparison of the measuring light values at the different measuring points of time; and determining the conclusion of the haemolysis when the gradient within a selectable measurement accuracy, after a measuring period in which the gradient is different from zero, falls to a minimum going down to zero. Another aspect of the invention relates to a device for the determination of the haemolysis of a blood sample. | 06-24-2010 |
| 20100137574 | SYSTEM AND METHOD FOR THE AUTOMATED EXTRACTION OF NUCLEIC ACIDS - A system and method for the automated extraction of nucleic acids from nucleic acids containing samples are disclosed. In the system, reagents provided in cavities of a reagent plate are transferred to samples accommodated in a process plate using a pipetting device comprising pipettes provided with disposable pipette tips for pipetting of the reagents to obtain sample-reagent mixtures, the sample-reagent mixtures accommodated in the process plate are incubated by an incubating device to release the nucleic acids; the released nucleic acids accommodated in the process plate are separated by a separating device and released to obtain extracted nucleic acids containing fluids; the extracted nucleic acids containing fluids are transferred to cavities of an output plate by disposable pipette tips; wherein each of the samples is assigned one-to-one to a cavity of the reagent plate, at least one of the disposable pipette tips and a cavity of the output plate. | 06-03-2010 |
| 20100136563 | SYSTEM AND METHOD FOR NUCLEIC ACIDS CONTAINING FLUID PROCESSING - A system and method for the processing of nucleic acids containing fluids involving manipulation of magnetically responsive particles contained therein are disclosed. In the system, a holder holds a plurality of containers containing the fluids, a heating device applies thermal energy to the fluids for incubation, and a separating device magnetically separates the particles. The heating and separating devices move into at least one operative position for processing the fluids and at least one inoperative position with respect to the containers, in which the containers are kept stationary at least during and in-between incubating the fluids and manipulating the magnetically responsive particles. | 06-03-2010 |
| 20100135824 | Process for Peristaltic Pump Control - A peristaltic pump is provided comprising squeezing elements moved by at least one actuator, which squeezing elements act on a tube in which a medium is conveyed, with the squeezing elements successively getting into and out of a squeezing engagement with the tube. A process for controlling the peristaltic pump comprises measuring over time a fluidic parameter representative for the flow rate of the medium through the tube, determining the relative undulation of the flow rate of the medium from the measured temporal course of the fluidic parameter, and smoothing the undulation by adjusting the progression speed of the squeezing elements on the basis of the determined undulation of the flow rate. | 06-03-2010 |
| 20100132487 | PIPETTING DEVICE, MODULAR PIPETTING UNIT, PIPETTING SYSTEM AND METHOD FOR PIPETTING OF FLUID SAMPLES - A pipetting device having a modular pipetting unit including a pipetting tip for pipetting of fluid samples and a pump conduit for transferring a negative or positive pressure to the pipetting tip is disclosed. The pipetting tip and a portion of the pump conduit adjoining the pipetting tip mutually define a fluid sample conduit for receiving the fluid samples. The modular pipetting unit is detachably attached to an automated positioning device for positioning the modular pipetting unit. A system and method for pipetting of fluid samples using such a pipetting device are also disclosed wherein pipetting of the fluid samples is performed in such a manner that each pipetted fluid sample volume is smaller than a volume of the fluid sample conduit. | 06-03-2010 |
| 20100132484 | SYSTEM AND METHOD FOR THE PROCESSING OF LIQUID SAMPLES - A method and system for automatically processing of liquid samples involving mixing of the samples with fluids are disclosed. The system includes a storing and handling device for storing and handling of fluid containers, which includes: a storing member provided with a plurality of storing positions, adapted for accommodating the fluid containers, the storing member having at least two storing levels, each of which extending in a plane, which are being stacked in a direction orthogonally aligned to the plane; and a handler, adapted for automatically transferring the fluid containers at least with respect to the storing positions. A method for operating such storing and handling device is also disclosed, wherein individual fluid containers are transferred between storing positions of a same or different storing levels in accordance with processing of the liquid samples. | 06-03-2010 |
| 20100132438 | SYSTEM AND METHOD FOR THE AUTOMATED PROCESSING OF FLUIDS, METHOD FOR DETERMINING THE MATCHING OF OBJECTS - A system and method for the automated processing of fluids according to a process operation plan involving the use of preloaded objects, which are to be present in target object positions, are disclosed. The system includes: a processing area in which objects to be used for the processing of fluids are located; at least one ultrasonic sensor for determining the presence of objects by acoustical waves; a positioning device to which the ultrasonic sensor is fixed and which moves the ultrasonic sensor in at least one direction relative to the processing area; a control computer determining the presence of objects and determining if objects are present in target object positions in the processing area as defined by the process operation plan; a pipetting device for pipetting of fluids between cavities located in the processing area; and an analytical or pre-analytical processing device for processing of fluids located in the processing area. | 06-03-2010 |
| 20100125589 | METHOD FOR GRAPHICALLY PROCESSING DISPLAYED DATA RECORDS FOR MINIMIZING A SELECTION ERROR RATE - A method for displaying and processing clinical data and a user interface are disclosed. In order to reduce the error rate in selecting a data record from a selection list displayed, data records that are displayed in the displayed selection list are automatically checked for similar displayed data records' representation, in which a similar displayed representation includes at least one displayed data record attribute that is identical or similar to the displayed data record attribute of said data type of another displayed data record. Similar displayed data records are additionally graphically processed upon displaying the selection list providing visual differentiation of similar record representations for the selection about to be made. | 05-20-2010 |
| 20100124779 | Two-Step Moulded Capillary - Reaction containers, such as plastic capillaries having an optimized volume-to-surface ratio that are suitable for real-time nucleic acid amplification (rtPCR) applications are disclosed as well as a method for the production of the reaction containers, in particularly the trtPCR plastic capillaries via a 2-step molding process. In the process, a capillary section is closed at one end, a tubular section is provided opened at both ends, and a linkage is provided between the capillary section and the tubular section, wherein the linkage is a fused joint designed to permanently link the open end of the capillary section to one of the open ends of the tubular section thus forming a reaction container having one opening, and in which the fused joint produces light scatter upon illumination. | 05-20-2010 |
| 20100113976 | SEALING CAP FOR A BODY FLUID CONTAINER AND A BLOOD COLLECTION DEVICE - A sealing cap for a body fluid container, and a body fluid collection device and system are disclosed. The sealing cap includes an inner cap placeable on an opening in the body fluid container forming a mouth, the inner cap has a shielding member which seals the mouth of the body fluid container, an outer cap resting on the inner cap, the outer cap being movable relative to the inner cap, and a channel member, wherein by a rotational movement the outer cap is movable between an first position in which the channel member is located separated from the shielding member and a second position in which the channel member extends through the shielding member, thereby establishing an open state of the shielding member, and wherein the shielding member returns to a closed state when the outer cap is moved back from the second position to the first position. | 05-06-2010 |
| 20100112717 | Method for Providing a Dried Reagent in a Microfluidic System and Microfluidic System - A method for providing a dried reagent in a microfluidic system is provided, the method comprising the following steps: providing a microfluidic system having a microfluidic structure, introducing a flowable carrier medium containing a reagent in the microfluidic structure, and drying the reagent in the microfluidic structure by lyophilization. | 05-06-2010 |
| 20100107743 | DEVICE AND METHOD FOR THE DETERMINATION OF AN ANALYTE IN A SAMPLE OF LIQUID - A device for determining an analyte in a sample of liquid comprises an analysis apparatus configured to analyze a sample of liquid applied to an analytical area of a test element. The device comprises further an apparatus configured to prepare a surface of the analytical area by conferring hydrophilic properties to the surface. Analytes in test samples are determined by methods employing the device. | 05-06-2010 |
| 20100077853 | METHOD AND APPARATUS FOR DETECTING CONTACT OF A PIPETTING NEEDLE WITH A LIQUID IN A VESSEL - A method and level sensor apparatus for detecting contact of a pipetting needle with at least a liquid contained in a vessel are disclosed. The apparatus provides a pipetting needle made of a material suitable for transmitting ultrasonic waves, a needle holder for holding the needle, a electromechanical transducer for generating ultrasonic pulses to be transmitted towards the needle, for receiving echo pulses reflected at the tip of the needle, and for generating an electrical output signal representative of the echo pulses, and electronic circuit means for generating and applying a driving signal to the transducer, which generates corresponding pulses which are transmitted to the needle towards the tip thereof, and for monitoring and evaluating the output signal to detect the position of the needle at which the tip of the needle contacts the liquid and for providing a resulting signal representative of the result of said evaluation. | 04-01-2010 |
| 20100076784 | PATIENT DIABETES DATA INTERCHANGE WITH ELECTRONIC MEDICAL RECORDS - A system and method for transferring patient diabetes information into an electronic medical record on a health record system with user validation are disclosed. After testing a patient's blood glucose levels over a period of time with a blood glucose meter which stores the patient diabetes information and the blood glucose levels in a first electronic format record, and after a user transfers the first electronic format record from the blood glucose meter into a diabetes management system on a computer, the invention provides a service which automatically monitors an output folder to determine when an export file containing the patient diabetes information is stored therein and after detection, automatically processes the export file into a default electronic medical report which can be copied into a clipboard utility provided by the computer and pasted into the electronic medical record of the patient on the health record system. | 03-25-2010 |
| 20100064781 | MULTI-WELL PLATE WITH TAILORED CHAMBERS - Systems, methods and multi-well plates comprising an array of wells for thermal treatment of chemical or biological samples are disclosed. Each of the wells comprises a bottom opening, an upper opening, inner side walls extending from the bottom opening to the upper opening, a protrusion extending from the inner side walls into the well with a first cross-sectional area and located at a height from the bottom opening which is smaller than the height from the upper opening. A sample chamber with a second cross-sectional area is formed between the bottom opening and the protrusion. An upper chamber with a third cross-sectional area is formed between the protrusion and the upper opening, and in which the first cross-sectional area is smaller than the third cross-sectional area and smaller than or equal to the second cross-sectional area. | 03-18-2010 |
| 20100064257 | INSULIN PUMP CONFIGURATION PROGRAMMING INVALID SETTINGS NOTIFICATION AND CORRECTION - An insulin pump configuration programming approach is disclosed that permits setting parameters of pump configuration files to invalid values. An operator may continue with the programming workflow after setting the invalid value. The configuration file including the invalid value may be saved to a memory location of a computing device, but cannot be saved to the pump. Invalid item icons are presented when a parameter is set to an invalid value, and instructions for correcting the invalidity condition are provided when an invalid item icon is hovered over using a pointing device. | 03-11-2010 |
| 20100063844 | EXTENSIBLE THERAPY DELIVERY SYSTEM AND METHOD THEREOF - An extensible therapy delivery system for an individual having a clinical rules module providing an existing clinical rule and is extensible to receive a new validated clinical rule and method thereof are disclosed. The extensible system also provides a domain module having existing clinical data and base logic and is extensible to receive new clinical data and additional logic to support the new validated clinical rules. The extensible system also provides a data request interface that directs a request for information from the clinical rules for the determination of therapy for the individual to the domain module, which answers the request with the existing and new clinical data and logic. The extensible system delivers to the individual the therapy determined by the clinical rules module from using the answer to the request provided by the domain module. | 03-11-2010 |
| 20100055770 | HIGH-DENSITY MULTIWELL-PLATE - A high-density multiwell-plate for performing thermocycled amplification reactions of polynucleotides in liquid samples comprising a plurality of reaction wells is disclosed. In order to provide a better thermal insulation, the plate comprises a rigid well-forming structure placed above a bottom layer, wherein substantially horizontal well-covering areas cover the liquid sample comprised in the wells, and a substantially plane cover placed above the well-forming structure providing a thermal insulating air distance between the well-covering areas and the cover. | 03-04-2010 |
| 20100050236 | QUALITY ASSURED ANALYTICAL TESTING SYSTEM AND METHOD THEREOF - A system and method for quality assured analytical testing is disclosed. A user is prompted by the system questions which relate to an analytical test to be conducted or an analytical instrument to be employed. Input received by the system from the user is evaluated to determine to which degree the inputs are correct. The user is certified if the determined degree is above a preset threshold. Next, the user is prompted by the system for a user identification and if the user is a certified user, access is provided to a testing routine of the analytical instrument. | 02-25-2010 |
| 20100044260 | PACKAGE FOR HYDROPHILIC MEDICAL INSTRUMENTS - The invention relates to a plastic package for hydrophilic articles, in particular for hydrophilically coated medical instruments, which package is intended to ensure the hydrophilic nature of the enclosed instrument over a long period of time. The package comprises at least one receiving compartment with a medical instrument for insertion into body tissue and is characterized in that, after sterilization by radiation, it has a proportion of volatile constituents of ≦0.1 μg/cm | 02-25-2010 |
| 20100028934 | PIPETTE TIP AND A METHOD FOR PIPETTING A CONGEALED BLOOD SAMPLE UTILIZING THE PIPETTE TIP - A pipette tip and a method for pipetting a congealed blood sample utilizing the pipette tip are disclosed. The pipette tip includes an attachment section configured to be attached to a dispensing device, a liquid containing section configured to receive at least part of an aspired liquid sample, and a liquid aspiration section that is connected to the liquid containing section. The liquid aspiration section has a distal end aspiration opening and at least one further aspiration opening in a side wall. | 02-04-2010 |
| 20100011887 | Device And Method For Separating A Liquid Component Of A Blood Sample, And Analyzer Apparatus Comprising Such A Device - A device for separating at least part of the liquid component of a blood sample and methods thereof are disclosed. Generally, the device includes a container body for receiving the blood sample, a layer of retaining porous material, a layer of separating permeable material. The retaining porous material retains non-liquid components of the blood sample after the non-liquid components have been subjected to centrifugal force which forces them through the separating permeable material into the retaining porous material. | 01-21-2010 |
| 20100000343 | COLLECTION OF LIQUID ANALYTICAL SAMPLES FOR CLINICAL ANALYTICAL PURPOSE AND DEVICE THEREOF - A method for collecting a sample volume containing at least one analyte of interest from a liquid analytical sample having undesired contaminants disposed at or near the sample surface, and an analytical device for performing the method are disclosed. The method comprises providing the sample, providing a first pipetting device comprising a first reusable pipetting needle which aspirates from an upper region of the liquid analytical sample a portion comprising the undesired contaminants and discards the portion, washing the first reusable needle with a washing liquid, providing a second pipetting device comprising a second reusable pipetting needle or a disposable pipetting tip which aspirates the sample volume from the liquid analytical sample after the first pipetting device discards the aspirated portion of the liquid analytical sample, and discharges the sample volume for analysis, and washing the second reusable needle with a washing liquid or disposing the disposable tip. | 01-07-2010 |
| 20090326357 | Method, system, and computer program product for calculating daily weighted averages of glucose measurements (or derived quantities) with time-based weights - A method and system for calculating daily weighted averages of glucose measurements (or derived quantities) with time-based weights are disclosed. The present invention computes an average daily glucose value using the time based weights based on only consecutive glucose measurements in the plurality of glucose measurements with acceptable time intervals that do not exceed a predefined maximum time interval. The invention further relates to a computer program for implementing the method for calculating daily weighted averages of spot monitoring glucose measurements (or derived quantities) with the time-based weights. | 12-31-2009 |
| 20090311796 | MICROFLUIDIC ANALYTICAL DEVICE FOR ANALYSIS OF CHEMICAL OR BIOLOGICAL SAMPLES, METHOD AND SYSTEM THEREOF - An analytical device for analysis of chemical or biological samples, a method of using such a device, based on rotation of the device, integrated sample dosing and optical detection, and a system comprising such a device are disclosed. The analytical device comprises a device body having a liquid processing unit. The liquid processing unit comprises a mixing chamber for mixing a sample with a reagent, a sample dosing chamber for delivering a defined volume of the sample to the mixing chamber, and a reagent channel for delivering the reagent to be mixed with the sample, wherein the mixing chamber also serves as a detection chamber. | 12-17-2009 |
| 20090286211 | MEDICAL DEVICE FOR VISUALLY IMPAIRED USERS AND USERS NOT VISUALLY IMPAIRED - The present invention refers to a medical device for self testing and monitoring the concentration of analytes in a body fluid, or a blood parameter, or for the controlled administration of therapeutic agents, comprising a connectable, preferably pluggable Braille or Braille-like module for visually impaired users, so that both visually impaired users and users not visually impaired can read the data generated by the medical device and/or control the medical device. | 11-19-2009 |
| 20090275861 | BODY FLUID TESTING DEVICE - Body fluid testing device for analyzing a body fluid comprises a test media tape adapted to collect the body fluid. The test media tape comprises a tape and test media portions. A free tape portion without test medium is located between successive test media portions. The testing device further comprises a supply portion. The supply portion comprises a housing in which uncontaminated test media tape is contained. The housing further has an opening for withdrawing test media tape from the housing. The testing device further has a sealing means for closing the opening against the surrounding. A free tape portion of the test media tape is located between a wall of the housing and the sealing means when the sealing means closes the opening. Further aspects concern a test media cassette with sealing means and a method for providing test media while holding them sealed against humidity during onboard storage. | 11-05-2009 |
| 20090263652 | HYDROPHILIC ADHESIVE COVER FOR COVERING FLUIDIC DEVICES - Embodiments of the present invention concerning an adhesive mixture having an acrylic adhesive and a detergent, an adhesive foil provided with the adhesive mixture, and a test element provided with the adhesive foil are disclosed. The adhesive mixture combines two properties, i.e. hydrophilicity and adhesiveness with one another, thereby making the adhesive mixture suitable for adhesive foils that are used as covers for fluidic devices. | 10-22-2009 |
| 20090220987 | Use of Intramolecularly, Covalently Cross-Linked Proteins As Binding Partners In Immunoassays - The invention concerns the use of intramolecularly, covalently cross-linked proteins and covalently cross-linked reverse transcriptase from HIV as immunological binding partners in immunoassays. It also concerns immunological test procedures for detecting an analyte in a sample in which intramolecularly, covalently cross-linked proteins are used as binding partners, and it further concerns intramolecularly, covalently cross-linked reverse transcriptase from HIV and a method for producing this reverse transcriptase. | 09-03-2009 |
| 20090216460 | METHOD TO DETERMINE THE DEGREE AND STABILITY OF BLOOD GLUCOSE CONTROL IN PATIENTS WITH DIABETES MELLITUS VIA CREATION AND CONTINUOUS UPDATING OF NEW STATISTICAL INDICATORS - Systems and methods for determining a stability of a blood glucose concentration of a patient are provided. The system comprises a processor that may be programmed to receive blood glucose concentration test results each taken from the patient at a different time over a time period and to compute a time-averaged glucose parameter indicative of blood glucose concentration control over the time period. In addition, the processor may be programmed to compute a virtual blood hemoglobin parameter through a simulated measurement of a blood hemoglobin, the virtual blood hemoglobin parameter being indicative of blood glucose concentration control over an extended time period encompassing the time period. Further, the processor may be programmed to compute a lability factor parameter indicative of a variability in blood glucose concentration over the time period. | 08-27-2009 |
| 20090208989 | Fluorescence Spectropscopy In Absorbing Media - The invention relates to processes and devices for detecting an analyte in a sample by fluorescence measurement. | 08-20-2009 |
| 20090198119 | PACKAGE FOR AN OBJECT HAVING A HYDROPHILIC SURFACE COATING - A package for an object having a hydrophilic surface includes at least one of a loose cover for the hydrophilic surface and an adsorbing surface, the affinity of which for apolar gases is equal to or greater than that of the hydrophilic surface. | 08-06-2009 |
| 20090192813 | INFORMATION TRANSFER THROUGH OPTICAL CHARACTER RECOGNITION - A medical data receiver configured to optically capture medical data, extract the medical data from the optical capture as alphanumeric characters, and provide the alphanumeric medical data for analysis. | 07-30-2009 |
| 20090191643 | Rotatable Test Element - A test element and method for detecting an analyte with the aid thereof is provided. The test element is essentially disk-shaped and flat, and can be rotated about a preferably central axis which is perpendicular to the plane of the disk-shaped test element. The test element has a sample application opening for applying a liquid sample, a capillary-active zone, in particular a porous, absorbent matrix, having a first end that is remote from the axis and a second end that is near to the axis, and a sample channel which extends from an area near to the axis to the first end of the capillary-active zone that is remote from the axis. | 07-30-2009 |
| 20090177427 | SYSTEM AND A METHOD FOR MANAGING SAMPLE TEST RESULTS AND RESPECTIVE SAMPLE RESULT CONTEXT INFORMATION - A system and method for managing sample test results and respective sample result context information within a laboratory environment are disclosed. The system provides an analytical unit configured to run at least one test on a sample, and a management unit connected with the analytical unit for data interchange, wherein said management unit is configured to save and display on demand sample test results and respective sample result context information, to control dynamically at least one actual value of at least one item of the respective sample result context information with respect to a scheduled threshold value and to initiate at least one action when the actual value corresponds to the scheduled threshold value according to a predefined execution plan schedule. Furthermore, embodiments referring to an appropriate management unit and a method for managing sample test results and respective sample result context information within a laboratory environment are also disclosed. | 07-09-2009 |
| 20090176314 | REAGENT CARTRIDGE - A reagent cartridge which can be exchangeably inserted into an analyzer and having a plurality of reagent bags furnished with connecting lines, each of which may optionally be connected to an input device of the analyzer, and method for operating the analyzer are disclosed. Each reagent bag has an analyzer-controlled multi-way valve with at least two valve positions at the point where the respective connecting line departs, such that the first valve position opens a fluid path between the connecting line and the reagent bag, while the second valve position closes off the reagent bag and opens a fluid path between a ventilation source, e.g. ambient air, and the connecting line. The connecting lines of the reagent bags departing from the multi-way valve open directly into a common rail or a collector valve. | 07-09-2009 |
| 20090155925 | MICROFLUIDIC ELEMENT FOR THOROUGHLY MIXING A LIQUID WITH A REAGENT - A microfluidic element for thoroughly mixing a liquid with a reagent used for the analysis of the liquid for an analyte contained therein and a method thereof are disclosed. The microfluidic element has a substrate and a channel structure. The channel structure includes an elongate mixing channel and an output channel. The mixing channel has an inlet opening and an outlet opening, and is implemented to mix the reagent contained therein with the liquid flowing through the inlet opening into the mixing channel. The outlet opening of the mixing channel is in fluid communication to the output channel. The outlet opening is positioned closer to the middle of the length of the mixing channel than the inlet opening. | 06-18-2009 |
| 20090155762 | Device and Method for Separating and Discharging Plasma - The invention concerns plasma separation on a microliter scale. The method/system according to the invention is able to provide plasma in the range of several microliters within a very short time as it is required, for example, in modern analyses by carrier-bound test elements. Plasma separation and plasma release is carried out in two separate consecutive steps of the method using the device according to the invention such that hemolysis during plasma separation can be avoided despite an accelerated procedure. The device comprises a disposable unit in which the device is characterized by an economical and simple method of production. | 06-18-2009 |
| 20090150877 | Data driven communication protocol grammar - An application software is provided which communicates with one or more resources having resource specific communication grammars. Grammar for each resource specific communication grammar is provided in a location external to the application software and is used by the application software to generate a communication stack for communicating with the respective resource. | 06-11-2009 |
| 20090150865 | Method and system for activating features and functions of a consolidated software application - A system and method for activating selected features and functions of a software application during installation of software. | 06-11-2009 |
| 20090150831 | Method and system for configuring a consolidated software application - A system and method for selectively configuring features and functions of a consolidated software application for particular end users. | 06-11-2009 |
| 20090150812 | Method and system for data source and modification tracking - A system and method for displaying data are disclosed, the method being applicable to a system comprising a computing device having an output device and software programs, and, optionally, an input device. The programs are configured to provide a screen display having display objects. The display objects distinguish the data according to the sources of the data. | 06-11-2009 |
| 20090150780 | Help utility functionality and architecture - A system and method is provided for displaying a first selectable indicia that, when selected, produces a document of first help information relating to a first topic. The system and method also displaying a second selectable indicia that, when selected, produces a document of second help information relating to a chapter that includes the first topic. | 06-11-2009 |
| 20090150771 | System and method for reporting medical information - A system and method for reporting medical information permits a user to output reports containing the information in multiple formats. The user can select report recipients, report templates and output formats. The report templates can be populated with data stored in a database. Different recipients can receive the reports in different formats and/or languages. Different recipients can also receive reports generated from the same template but containing different data. | 06-11-2009 |
| 20090150758 | Method and system for creating user-defined outputs - A system and method for creating a template configured to generate reports for reporting medical information. The method allows a user to generate a single template that may be then utilized in order to create a plurality of reports for numerous patients. The template is created by dragging and dropping the desired information onto a blank report. Once the desired format of the template has been set by the user, the user may save the template for future use. | 06-11-2009 |
| 20090150683 | Method and system for associating database content for security enhancement - A system and method for associating database content for security enhancement is provided, the method being applicable to a system comprising a computer configured to process a data management application and to store data in databases. According to one embodiment of the method according to the invention, the application uses an encryption key to encrypt data. The application stores the encrypted data in two or more databases. The databases may comprise a system database for storing encrypted user access data and one or more results databases for storing patient data. Databases may be stored locally, remotely, or both locally and remotely. | 06-11-2009 |
| 20090150549 | Dynamic communication stack - A method of facilitating communication between a resource and a computer is described. The computer employs a software application that allows the computer to communicate with the resource. The resource may comprise a medical device such as a blood glucose meter or an insulin pump. In order to facilitate communication between the computer and the resource, the software constructs a communication protocol particular to the type of resource connected to the computer. The stack comprising the communication protocol allows the computer to communicate with the resource. Once the resource and computer cease communication, the stack may be removed from the memory of the computer. | 06-11-2009 |
| 20090150482 | Method of cloning a server installation to a network client - A medical data system wherein a server installation identifies configuration choices and creates a client installer that will install a cloned application on client machines that conforms to the configuration choices made during the server installation. | 06-11-2009 |
| 20090150454 | System and method for database integrity checking - A method is disclosed for checking the integrity of a database through a test of database integrity information provided in the database and integrity information provided external to the database. The integrity information may be provided in a configuration file. | 06-11-2009 |
| 20090150451 | Method and system for selective merging of patient data - A method and system for merging patient data in the form of medical information, e.g., patient and/or healthcare provider information, is provided, which may be utilized to identify medical information stored in a first location that is unique to, a duplicate of, and/or a potential duplicate of medical information stored in a second location. In one exemplary embodiment, the present invention is utilized in conjunction with or incorporated into medical management software. In one exemplary embodiment, the medical management software is disease management software, such as diabetes management software. In medical management software, it is important to ensure that specific, individual records containing medical information are properly associated with an individual patient and/or healthcare provider. | 06-11-2009 |
| 20090150440 | Method and system for data selection and display - A method and apparatus for concurrently displaying sets of data related to a medical condition, including a feature which enables the user to select one or more of the data sets for emphasized or more prominent display relative to the other data set(s). | 06-11-2009 |
| 20090150439 | Common extensible data exchange format - A medical data system wherein data is exchanged internally and externally by a common data exchange format. | 06-11-2009 |
| 20090150438 | Export file format with manifest for enhanced data transfer - An export file format and a method and system for creating and accessing an export file. In one embodiment, the system includes a facility to import and export databases, in whole or in part. In one exemplary embodiment, the export files are used for transferring information between databases. In another exemplary embodiment, the export files are used to archive portions of databases. | 06-11-2009 |
| 20090150416 | Method and system for enhanced data transfer - A system and method for enhanced data transfer are disclosed, the method being applicable to a system comprising a computing device configured to transfer data from a portable device. In one embodiment, the computing device stores a fingerprint of the newest record downloaded from a portable device and stops downloading records from the device when a downloaded record matches the fingerprint. In another embodiment, the computing device stores a fingerprint of the newest record downloaded from a portable device and fully processes records that are downloaded from the device after a downloaded record matches the fingerprint. The system may include a portable device configured to adapt its operation responsive to a system fingerprint provided by the computing device. The portable device may be a medical device. The system may be a healthcare data management system. | 06-11-2009 |
| 20090150377 | Method and system for merging extensible data into a database using globally unique identifiers - A method of merging data from one database into another database uses metadata identifiers to indicate the type of data. One of the databases can be stored on a medical device, and the other of the databases can be stored on a computer. When transferring data from the first database to the second database, the metadata identifiers are used to identify and merge common data types. | 06-11-2009 |
| 20090150351 | Method and system for querying a database - A method and system for querying a database involves dragging and dropping selected search criteria from one portion of a display to another portion of a display. When searching multiple criteria, a Boolean operation associated with the method depends upon the respective positions of the search criteria in the display. The method also allows for the results of the search to be dynamically updated as different criteria are selected. | 06-11-2009 |
| 20090150331 | Method and system for creating reports - A system and method for reporting medical information permits a user to produce reports by storing report templates in a database, selecting at least two of the report templates and storing the selected report templates in the database as a new report template. The user can also change parameters associate with the previously stored report templates when creating the new report template. | 06-11-2009 |
| 20090150181 | Method and system for personal medical data database merging - A method and system for merging databases containing medical, patient and/or healthcare, information is provided, which may be utilized to merge a source database containing medical information into a new or existing destination database. The method may include the steps of identifying a source database containing medical information, identifying a destination database for the receipt of the medical information from the source database, selecting rules for governing the migration of medical information into the destination database, and migrating the medical information from the source database to the destination database. In one exemplary embodiment, the medical information is a plurality of individual patient's medical records. In another exemplary embodiment, the medical information is a plurality of healthcare provider records. | 06-11-2009 |
| 20090150177 | Method and system for setting time blocks - A method and system for setting time blocks of a repeating time period is disclosed. The method and system may be a part of a healthcare management software system. | 06-11-2009 |
| 20090150176 | Patient-centric healthcare information maintenance - A system for facilitating patient centric healthcare information maintenance. For example, a health management software system may be operated to receive, organize, and use patient medical information. The health management software may comprise a database for storing, retrieving, organizing, displaying, and, generally, for managing a patient's health. In one exemplary embodiment, the health management software system is used in conjunction with a healthcare maintenance device, such as a blood glucose monitoring system. The blood glucose monitoring system may contain several database objects in the form of data records. Typically in a portable blood glucose monitor, each data record contains a time and a concentration data element, or a time-amount point. Similarly, an insulin pump, which is another exemplary embodiment of a healthcare maintenance device, may maintain data records with time and dosage information, or a time-dosage point. | 06-11-2009 |
| 20090150175 | Method and system for multi-device communication - A medical data system including a plurality of receivers configured to wirelessly receive medical data via a signal. | 06-11-2009 |
| 20090150174 | Healthcare management system having improved printing of display screen information - A healthcare management system generates stylized reports of the physiological information from a display portion of the user interface using a pre-formatted report structure for each of a plurality of different display screens. | 06-11-2009 |
| 20090149131 | Method and system for wireless device communication - A medical data receiver configured to wirelessly receive medical data via a signal and having an externally perceptible indicator of signal reception. | 06-11-2009 |
| 20090147026 | Graphic zoom functionality for a custom report - The present invention relates to a software zoom feature capable of magnifying data plotted on a graph. The graph may display any type of data including medical data. The graph may also be customizable as to the type of data displayed. The data that is to be magnified by the zoom feature may be selected using a click and drag technique with an input device, such as a mouse, connected to a computer. | 06-11-2009 |
| 20090147011 | Method and system for graphically indicating multiple data values - A system and method for displaying data are disclosed, the method being applicable to a system comprising a computing device having an output device and computer programs, and, optionally, an input device. The programs are configured to show point display objects and group display objects corresponding to data points located near each other. The group display objects are distinguishable from the point display objects. | 06-11-2009 |
