Patent application number | Description | Published |
20080281278 | INJECTOR DEVICE, METHOD, AND COMPUTER PROGRAM PRODUCT FOR DETECTING A VACUUM WITHIN A SYRINGE - An injector system, method and computer program product for detecting a vacuum within a syringe are provided. Various embodiments include an actuator device configured to be engaged with a piston member of a syringe for extending and retracting the piston member within the syringe. A controller device is also provided for detecting an output generated by the actuator device when retracting the piston member. The detected output may be associated with a pressure within the reservoir. The controller device determines, via the detected output, when the pressure comprises a selected negative pressure and provides an indicia of the negative pressure to a user and/or a signal to the actuator device. | 11-13-2008 |
20090171268 | Manually Operated Insufflator - The invention includes a device, kit, and system capable of manually distending a subject's body cavity. In one embodiment, the invention includes a distention media reservoir ( | 07-02-2009 |
20110034862 | INSUFFLATING SYSTEM, METHOD, AND COMPUTER PROGRAM PRODUCT FOR CONTROLLING THE SUPPLY OF A DISTENDING MEDIA TO AN ENDOSCOPIC DEVICE - The present invention is directed to a system, method, and computer program product for controlling the supply of a distending media (such as an insufflating gas) from a distending media source to an endoscopic device so as to prevent the excess venting and/or waste of distending media. More specifically, the present invention provides for the detection of a pressure level within a lumen of an endoscopic device and adjusts a supply parameter of the distending media based at least in part on the detected pressure level, and in some cases, on the relationship between the detected pressure level and a user-defined threshold. | 02-10-2011 |
20120157770 | Insufflating System, Method, And Computer Program Product For Controlling The Supply Of A Distending Media To An Endoscopic Device - The present invention is directed to a system, method, and computer program product for controlling the supply of a distending media (such as an insufflating gas) from a distending media source to an endoscopic device so as to prevent the excess venting and/or waste of distending media. More specifically, the present invention provides for the detection of a pressure level within a lumen of an endoscopic device and adjusts a supply parameter of the distending media based at least in part on the detected pressure level, and in some cases, on the relationship between the detected pressure level and a user-defined threshold. | 06-21-2012 |
20130102882 | SYSTEM, IMAGING SUITE, AND METHOD FOR USING AN ELECTRO-PNEUMATIC INSUFFLATOR FOR MAGNETIC RESONANCE IMAGING - Embodiments of the invention provide a system and method for using an electro-pneumatic insufflator for magnetic resonance imaging, such as for virtual colonoscopy. Embodiments of the invention further provide a MRI imaging suite and a method for distension of a body part to be imaged. As an alternative to the complete redesign of an electro-magnetic insufflator, embodiments of the current invention utilize a standard electro-pneumatic insufflator that operates in a location impervious to electromagnetic radiation using an electromagnetically inactive connection tube. | 04-25-2013 |
20140154670 | VALIDATION TECHNIQUES FOR FLUID DELIVERY SYSTEMS - A fluid delivery system may include a container that houses a medical fluid, a fluid pressurizing unit, and a fluid transfer set that transfers the medical fluid from the container to the fluid pressurizing unit. To validate the integrity and sterility of the fluid delivery system, the system may undergo testing protocols to evaluate the susceptibility of the system to pathogenic ingress, chemical degradation, and/or fluid cross-contamination between patient fluid delivery procedures. The testing protocols may help ensure that delivery system components used during multiple different fluid delivery procedures perform as well as if the components were replaced after each fluid delivery procedure. | 06-05-2014 |
20140154671 | VALIDATION TECHNIQUES FOR FLUID DELIVERY SYSTEMS - A fluid delivery system may include a container that houses a medical fluid, a fluid pressurizing unit, and a fluid transfer set that transfers the medical fluid from the container to the fluid pressurizing unit. To validate the integrity and sterility of the fluid delivery system, the system may undergo testing protocols to evaluate the susceptibility of the system to pathogenic ingress, chemical degradation, and/or fluid cross-contamination between patient fluid delivery procedures. The testing protocols may help ensure that delivery system components used during multiple different fluid delivery procedures perform as well as if the components were replaced after each fluid delivery procedure. | 06-05-2014 |
20140301912 | VALIDATION TECHNIQUES FOR FLUID DELIVERY SYSTEMS - A fluid delivery system may include a container that houses a medical fluid, a fluid pressurizing unit, and a fluid transfer set that transfers the medical fluid from the container to the fluid pressurizing unit. To validate the integrity and sterility of the fluid delivery system, the system may undergo testing protocols to evaluate the susceptibility of the system to pathogenic ingress, chemical degradation, and/or fluid cross-contamination between patient fluid delivery procedures. The testing protocols may help ensure that delivery system components used during multiple different fluid delivery procedures perform as well as if the components were replaced after each fluid delivery procedure. | 10-09-2014 |
20140301913 | VALIDATION TECHNIQUES FOR FLUID DELIVERY SYSTEMS - A fluid delivery system may include a container that houses a medical fluid, a fluid pressurizing unit, and a fluid transfer set that transfers the medical fluid from the container to the fluid pressurizing unit. To validate the integrity and sterility of the fluid delivery system, the system may undergo testing protocols to evaluate the susceptibility of the system to pathogenic ingress, chemical degradation, and/or fluid cross-contamination between patient fluid delivery procedures. The testing protocols may help ensure that delivery system components used during multiple different fluid delivery procedures perform as well as if the components were replaced after each fluid delivery procedure. | 10-09-2014 |