A system and method are disclosed for positioning a patient on an operating table. The patient positioning system includes a positioning pad having a body formed from a compressible material, a first end and a second end. The body has a thickness which increases from the first end of the positioning pad to the second end of the positioning pad. A plurality of tethers may be fixedly secured to the body. Each of the tethers may include a fastening member adapted to secure the body to an operating table. The positioning pad may include a perforated section to mirror a perineal cutout of an operating table.
An apparatus and method for delivering fluid from a syringe to a subject using a pumping device of a flow control apparatus. The method includes locating the flow control apparatus on a horizontal support surface. Providing the syringe with a volume of fluid including a total amount of preferred nutrient and an amount of non-preferred nutrient liquid. Mounting the syringe relative to the flow control apparatus whereby the syringe is oriented in a generally vertical orientation such that an outlet of the syringe faces upward. Initiating operation of the pumping device to draw the fluid from the syringe for a duration of time to preferentially deliver at least a portion of the total amount of preferred nutrient in the fluid to the subject.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/145 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons
An adapter assembly includes a tapered connector including a central passage and a tapered outer surface for sealing with a tube or bottle. A male connector for connection to a female connector to fluidly communicate the female connector with the tube or bottle is coupled with the tapered connector. A method of forming such an adapter assembly is also disclosed.
A biomedical connector includes a housing defining an interior space and an opening dimensioned to receive an electrode at least partially into the interior space. A lever is movably attached to the housing and biased toward an engagement position for contacting the electrode when the electrode is received in the opening in the housing to retain the biomedical connector to the electrode. A dampener is disposed in the interior space of the housing and configured to engage the electrode when the electrode is received in the opening in the housing. The dampener is configured to limit movement of the biomedical connector relative to the electrode to reduce motion artifact in a biomedical signal received by the biomedical connector.
A biomedical connector includes a housing defining an interior space and an opening dimensioned to receive an electrode at least partially into the interior space. A lever is movably attached to the housing and biased toward an engagement position for contacting the electrode when the electrode is received in the opening in the housing to retain the biomedical connector to the electrode. A dampener is disposed in the interior space of the housing and configured to engage the electrode when the electrode is received in the opening in the housing. The dampener is configured to limit movement of the biomedical connector relative to the electrode to reduce motion artifact in a biomedical signal received by the biomedical connector.
An apparatus and method for delivering fluid from a syringe to a subject using a pumping device of a flow control apparatus. The method includes locating the flow control apparatus on a horizontal support surface. Providing the syringe with a volume of fluid including a total amount of preferred nutrient and an amount of non-preferred nutrient liquid. Mounting the syringe relative to the flow control apparatus whereby the syringe is oriented in a generally vertical orientation such that an outlet of the syringe faces upward. Initiating operation of the pumping device to draw the fluid from the syringe for a duration of time to preferentially deliver at least a portion of the total amount of preferred nutrient in the fluid to the subject.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/145 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons
8.
SYSTEM, METHOD, AND DEVICE UTILIZING REVERSIBLE CONNECTOR
A method of reprocessing a compression garment including tubing and a connector attached to the tubing and in fluid communication with the tubing includes attaching a reprocessing cap to the connector, and performing a reprocessing procedure to clean, sanitize, and/or disinfect the compression garment whereby the reprocessing cap prevents ingress of fluid into the tubing of the compression garment.
A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.
A61F 13/84 - Accessoires, non prévus ailleurs, pour garnitures absorbantes
A61L 15/46 - Désodorisants ou produits pour neutraliser les mauvaises odeurs, p. ex. pour inhiber la formation d'ammoniac ou la multiplication de bactéries
A pump set for use with a pumping apparatus includes tubing for carrying a liquid. A valve mechanism is mounted to the tubing between an inlet section and a pump engagement section. The valve mechanism includes a first port connected to the inlet section of the tubing, a second port connected to the pump engagement section of the tubing, and a valve disposed between the first and second ports. The valve includes a stem rotatably mounted within a stem holder. The stem includes a flow passage extending through the stem and having an open V shape whereby a narrow open end of the flow passage communicates with the first port and a wide open end of the flow passage communicates with the second port to place the inlet section of the tubing in communication with the pump engagement section of the tubing.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A flow control apparatus comprising a housing capable of receiving a portion of the feeding set, a pumping device configured to receive the feeding set and may produce a fluid flow in the feeding set and deliver fluid to a subject, an ultrasonic sensor may be configured to produce a sensor signal indicative of a condition of the feeding set, and a control circuit in communication with the ultrasonic sensor for receiving the sensor signal from the ultrasonic sensor indicative of the condition of the feeding set. The ultrasonic sensor may comprise a plurality of sensor components which may be configured to emit an ultrasonic signal in a first direction, and in a second direction opposite the first direction through the feeding set.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
12.
SYSTEM, METHOD AND DEVICE FOR MONITORING AND EXPRESSING COMPLIANCE OF A MEDICAL TREATMENT
A compression garment controller and a method for monitoring compliance of a user wearing a compression garment wrapped around a limb of the user in accordance with a compression therapy. The method comprising directing a flow of fluid from a pressurized fluid flow source to cyclically inflate and deflate an inflatable bladder of the compression garment; receiving pressure signals indicative of fluid pressure in the inflatable bladder from a pressure sensor communicatively coupled thereto during at least one of inflation and deflation of the inflatable bladder in a plurality of successive compression cycles; processing the received pressure signals to determine compliance or non-compliance with the compression therapy; causing at least one a light emitting diode (LED) to illuminate in a first color indicating compliance with the compression therapy; and causing the at least one LED to illuminate in a second color indicating non-compliance with the compression therapy.
A compression garment controller and a method for monitoring compliance of a user wearing a compression garment wrapped around a limb of the user in accordance with a compression therapy. The method comprising directing a flow of fluid from a pressurized fluid flow source to cyclically inflate and deflate an inflatable bladder of the compression garment; receiving pressure signals indicative of fluid pressure in the inflatable bladder from a pressure sensor communicatively coupled thereto during at least one of inflation and deflation of the inflatable bladder in a plurality of successive compression cycles; processing the received pressure signals to determine compliance or non-compliance with the compression therapy; causing at least one a light emitting diode (LED) to illuminate in a first color indicating compliance with the compression therapy; and causing the at least one LED to illuminate in a second color indicating non-compliance with the compression therapy.
In one example, a sensor system of a patient monitoring system includes a voiding sensor that includes an electrical circuit configured to be transitioned from a first impedance state to a second impedance state in response to a voiding event in an absorbent region of an absorbent article worn by a patient. The sensor system also includes one or more processors configured to: determine, based on whether the impedance state of the electrical circuit is open or closed, that the voiding event has occurred; and generate, based at least in part on the occurrence of the voiding event, patient status data of the patient. The sensor system also includes a communication module configured to wirelessly transmit, via a relay module, the patient status data to a remote monitoring device that is distinct from the relay module.
A61F 13/42 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons avec un indicateur ou une alarme d'humidité
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.
A61F 13/84 - Accessoires, non prévus ailleurs, pour garnitures absorbantes
A61L 15/46 - Désodorisants ou produits pour neutraliser les mauvaises odeurs, p. ex. pour inhiber la formation d'ammoniac ou la multiplication de bactéries
17.
ENTERAL FEEDING SYRINGE INSTALLATION AND DETECTION
A device and method of controlling a device. The device may include a controller for controlling operation of a pumping device to producing a flow of fluid in the pump set, the controller including a processor and a memory, the controller being adapted to store in the memory, syringe size data, the controller configured to execute in the processor a syringe detection program to determine a presence and size of the syringe loaded onto a flow control apparatus.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A device and method of controlling a device. The device may include a controller for controlling operation of a pumping device to producing a flow of fluid in the pump set, the controller including a processor and a memory, the controller being adapted to store in the memory, syringe size data, the controller configured to execute in the processor a syringe detection program to determine a presence and size of the syringe loaded onto a flow control apparatus.
A flow control system and method of detecting a condition of a pump set mounted on the apparatus. The system configured to perform the method of advancing a first amount of the feeding formula through the feeding pump via a feeding formula conduit. Further, the system may acquire a first pressure sensor reading of the feeding formula conduit. Further, the system may advance a second amount of the feeding formula through the feeding pump via the feeding formula conduit, wherein the second amount is second volume of the liquid. Further, the system may acquire a second pressure sensor reading of the feeding formula conduit, and acquire a third pressure sensor reading of the feeding formula conduit. Further, the system may detect an occlusion in the feeding formula conduit based on at least one of the first pressure sensor reading, the second pressure sensor reading and the third pressure sensor reading.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
20.
OCCLUSION DETECTION SYSTEM AND METHOD FOR A FLOW CONTROL APPARATUS
A flow control system and method of detecting a condition of a pump set mounted on the apparatus. The system configured to perform the method of advancing a first amount of the feeding formula through the feeding pump via a feeding formula conduit. Further, the system may acquire a first pressure sensor reading of the feeding formula conduit. Further, the system may advance a second amount of the feeding formula through the feeding pump via the feeding formula conduit, wherein the second amount is second volume of the liquid. Further, the system may acquire a second pressure sensor reading of the feeding formula conduit, and acquire a third pressure sensor reading of the feeding formula conduit. Further, the system may detect an occlusion in the feeding formula conduit based on at least one of the first pressure sensor reading, the second pressure sensor reading and the third pressure sensor reading.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A cassette for use with a pumping apparatus having a pumping system for engaging a pump set includes a cassette body configured for releasable attachment to the pumping apparatus to mount the cassette on the pumping apparatus. The cassette body has at least one mounting formation. At least one identification member is mounted on the cassette body by the mounting formation of the cassette body. The identification member and mounting formation are formed to mount the identification member in any one of a plurality of predetermined orientations. Each predetermined orientation indicates a different functional configuration of the pump set.
A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.
A61F 13/00 - Bandages ou pansementsGarnitures absorbantes
A61L 15/46 - Désodorisants ou produits pour neutraliser les mauvaises odeurs, p. ex. pour inhiber la formation d'ammoniac ou la multiplication de bactéries
A61F 13/84 - Accessoires, non prévus ailleurs, pour garnitures absorbantes
Monitoring vital parameters of a wearer of a compression garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Analyzing the pressure signal waveform for an oscillating amplitude as a function of time and/or a representation of a pulse of the wearer provides an indication of blood pressure of the wearer.
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
The present disclosure provides articles having an absorbent core with a plurality of segmented volumes defined by a network of filaments, with an absorbent material therein. Suitable articles which may be formed with this absorbent core include, for example, diapers such as infant diapers, juvenile diapers and training pants, feminine hygiene products such as menstrual pads, adult incontinence products such as adult briefs, protective underwear, pads and bladder control pads, pet training pads, and other disposable products utilized to absorb fluids.
A61L 15/24 - Composés macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneLeurs dérivés
A61L 15/20 - Bandages, pansements ou garnitures absorbant les fluides physiologiques tels que l'urine, le sang, p. ex. serviettes hygiéniques, tampons contenant des matériaux organiques
A61F 13/539 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant caractérisées par la liaison des couches absorbantes entre elles ou avec les couches extérieures
A61F 13/534 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant ayant une composition non homogène sur toute l'épaisseur du noyau absorbant
A61F 13/535 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant ayant une composition non homogène sur toute l'épaisseur du noyau absorbant non homogène dans le plan de la garniture absorbante, p. ex. les couches absorbantes du noyau étant de différentes tailles
Monitoring patient compliance with a compression therapy regimen. Venous Refill Time (VRT) is monitored via a pressure sensor in a bladder of a compression system. A controller of the compression system correlates the monitored VRT to a predetermined threshold to determine whether the patient is using the compression system.
Medical devices, namely, sequential compression and therapeutic systems consisting of controller and tubing for the prevention of deep vein thrombosis.
An apparatus and method for delivering liquid to a subject using a pumping device of a flow control apparatus. The method includes recognizing a pump set including a liquid container with a volume of liquid mounted to the flow control apparatus whereby the pump set is positioned to be acted on by the pumping device to deliver aliquots of liquid through the pump set. Operation of the pumping device is initiated to draw a prescribed volume of the liquid from the liquid container for a duration of time. A single aliquot of the volume of liquid is delivered from the liquid container to the subject. Operation of the pumping device is paused for a predetermined period of time before delivering another single aliquot of the volume of liquid from the liquid container to the subject.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
An apparatus and method for delivering liquid to a subject using a pumping device of a flow control apparatus. The method includes recognizing a pump set including a liquid container with a volume of liquid mounted to the flow control apparatus whereby the pump set is positioned to be acted on by the pumping device to deliver aliquots of liquid through the pump set. Operation of the pumping device is initiated to draw a prescribed volume of the liquid from the liquid container for a duration of time. A single aliquot of the volume of liquid is delivered from the liquid container to the subject. Operation of the pumping device is paused for a predetermined period of time before delivering another single aliquot of the volume of liquid from the liquid container to the subject.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
An apparatus and method for delivering liquid to a subject using a pumping device of a flow control apparatus. The method includes recognizing a pump set including a liquid container with a volume of liquid mounted to the flow control apparatus whereby the pump set is positioned to be acted on by the pumping device to deliver aliquots of liquid through the pump set. Operation of the pumping device is initiated to draw a prescribed volume of the liquid from the liquid container for a duration of time. A single aliquot of the volume of liquid is delivered from the liquid container to the subject. Operation of the pumping device is paused for a predetermined period of time before delivering another single aliquot of the volume of liquid from the liquid container to the subject.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/172 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte électriques ou électroniques
A system and method are disclosed for positioning a patient on an operating table. The patient positioning system includes a positioning pad having a body formed from a compressible material including a slip-resistant surface. The body has a thickness which increases from a first end of the positioning pad to a second end of the positioning pad. A plurality of tethers are fixedly secured to the body. Each of the tethers includes a fastening member adapted to secure the body to an operating table.
09 - Appareils et instruments scientifiques et électriques
Produits et services
Laboratory instruments, namely, tissue grinder kits comprised of tissue collection tubes, grinder and sterile peel pouch for storing and disposing of the collection tubes and grinder
42.
MULTIPARAMETER LEAD SET AND METHODS OF USE THEREOF
A multiparameter lead set, method of use, and method of assembling or re-processing a multiparameter lead set. The multiparameter lead set includes a first patient lead for monitoring a first health indicator of a patient. The first patient lead further includes a first lead interconnection feature. The lead set further includes a second patient lead for monitoring a second health indicator of the patient. The second patient lead further include a second lead interconnection feature. The second lead interconnection feature and the first lead interconnection feature are interconnectable to removably connect a first portion of the first patient lead to a second portion of the second patient lead.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/01 - Mesure de la température de parties du corps
A61B 5/02 - Détection, mesure ou enregistrement en vue de l'évaluation du système cardio-vasculaire, p. ex. mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin
A61B 5/103 - Dispositifs de mesure pour le contrôle de la forme, du dessin, de la dimension ou du mouvement du corps ou de parties de celui-ci, à des fins de diagnostic
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
43.
MULTIPARAMETER LEAD SET AND METHODS OF USE THEREOF
A multiparameter lead set, method of use, and method of assembling or re-processing a multiparameter lead set. The multiparameter lead set includes a first patient lead for monitoring a first health indicator of a patient. The first patient lead further includes a first lead interconnection feature. The lead set further includes a second patient lead for monitoring a second health indicator of the patient. The second patient lead further include a second lead interconnection feature. The second lead interconnection feature and the first lead interconnection feature are interconnectable to removably connect a first portion of the first patient lead to a second portion of the second patient lead.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/01 - Mesure de la température de parties du corps
A61B 5/02 - Détection, mesure ou enregistrement en vue de l'évaluation du système cardio-vasculaire, p. ex. mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin
A61B 5/103 - Dispositifs de mesure pour le contrôle de la forme, du dessin, de la dimension ou du mouvement du corps ou de parties de celui-ci, à des fins de diagnostic
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
44.
MULTIPARAMETER LEAD SET AND METHODS OF USE THEREOF
A multiparameter lead set, method of use, and method of assembling or re-processing a multiparameter lead set. The multiparameter lead set includes a first patient lead for monitoring a first health indicator of a patient. The first patient lead further includes a first lead interconnection feature. The lead set further includes a second patient lead for monitoring a second health indicator of the patient. The second patient lead further include a second lead interconnection feature. The second lead interconnection feature and the first lead interconnection feature are interconnectable to removably connect a first portion of the first patient lead to a second portion of the second patient lead.
A feeding set for use with a peristaltic enteral feeding pump to deliver nutritional liquid fluid to a patient includes a container having nutritional liquid. A conduit assembly includes tubing placeable in fluid communication with the container and adapted for mounting on the enteral feeding pump. The tubing provides a fluid pathway for delivering the nutritional liquid from the container to a patient when the tubing is mounted on the enteral feeding pump. An identification member is mounted on the conduit assembly and has at least one characteristic of a nutritional liquid associated with the feeding set represented by the identification member. The identification member is positioned on the conduit assembly so as to permit automatic identification by the enteral feeding pump of the at least one characteristic of the nutritional liquid upon mounting the conduit assembly on the enteral feeding pump.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G16H 20/60 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant le contrôle de l’alimentation, p. ex. les régimes
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
A feeding set for use with a peristaltic enteral feeding pump to deliver nutritional liquid fluid to a patient includes a container having nutritional liquid. A conduit assembly includes tubing placeable in fluid communication with the container and adapted for mounting on the enteral feeding pump. The tubing provides a fluid pathway for delivering the nutritional liquid from the container to a patient when the tubing is mounted on the enteral feeding pump. An identification member is mounted on the conduit assembly and has at least one characteristic of a nutritional liquid associated with the feeding set represented by the identification member. The identification member is positioned on the conduit assembly so as to permit automatic identification by the enteral feeding pump of the at least one characteristic of the nutritional liquid upon mounting the conduit assembly on the enteral feeding pump.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
G16H 20/60 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant le contrôle de l’alimentation, p. ex. les régimes
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
(1) Medical devices, namely, sequential compression and therapeutic systems consisting of controller, liners and tubing for the prevention of deep vein thrombosis.
49.
Feed-fortify enteral feeding and related methods therefor
A pump set for use with a pumping apparatus to deliver nutrition to an infant includes a first container to receive breast milk; a second container to receive fortifier; tubing extending from the first container and from the second container; and a valve mechanism connected to the first and second containers by the tubing and configured to selectively pass liquid from the first container and the second container.
Determining whether a compression garment is worn by a wearer of the garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Variance detected in the pressure signal waveform during the analysis is indicative of a change in condition of the compression garment. In one aspect the change in condition is verified using confirmatory analysis. In another aspect, the variance is one of a pressure rise and a pressure impulse. In yet another aspect, the variance is an oscillating amplitude as a function of time representative of a pulse of the wearer.
A61F 5/01 - Dispositifs orthopédiques, p. ex. dispositifs pour immobiliser ou pour exercer des pressions de façon durable pour le traitement des os fracturés ou déformés, tels que éclisses, plâtres orthopédiques ou attelles
G01F 1/34 - Mesure du débit volumétrique ou du débit massique d'un fluide ou d'un matériau solide fluent, dans laquelle le fluide passe à travers un compteur par un écoulement continu en utilisant des effets mécaniques en mesurant la pression ou la différence de pression
medical devices, namely, sequential compression and therapeutic systems consisting of controller, liners and tubing for the prevention of deep vein thrombosis
Medical devices, namely, sequential compression and therapeutic systems consisting of controller, sleeves, liners and tubing for the prevention of deep vein thrombosis.
53.
SYSTEM, METHOD, AND DEVICE UTILIZING REVERSIBLE CONNECTOR
A compression garment that is selectively engageable and operable by a controller for inflation via a reversible connector, the compression garment comprising a plurality of bladders and compression garment tubing. The compression garment tubing includes a plurality of garment tubes in fluid communication with the plurality of bladders at a first compression garment tubing end and includes a second compression garment tubing end opposite the first compression garment tubing end. The reversible connector has a first connector portion and second connector portion, the first connector portion and the second connector portion being selectively reversibly connectable together to form the reversible connector.
A flow control apparatus comprising a housing capable of receiving a portion of the feeding set, a pumping device configured to receive the feeding set and may produce a fluid flow in the feeding set and deliver fluid to a subject, an ultrasonic sensor may be configured to produce a sensor signal indicative of a condition of the feeding set, and a control circuit in communication with the ultrasonic sensor for receiving the sensor signal from the ultrasonic sensor indicative of the condition of the feeding set. The ultrasonic sensor may comprise a plurality of sensor components which may be configured to emit an ultrasonic signal in a first direction, and in a second direction opposite the first direction through the feeding set.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A flow control apparatus comprising a housing capable of receiving a portion of the feeding set, a pumping device configured to receive the feeding set and may produce a fluid flow in the feeding set and deliver fluid to a subject, an ultrasonic sensor may be configured to produce a sensor signal indicative of a condition of the feeding set, and a control circuit in communication with the ultrasonic sensor for receiving the sensor signal from the ultrasonic sensor indicative of the condition of the feeding set. The ultrasonic sensor may comprise a plurality of sensor components which may be configured to emit an ultrasonic signal in a first direction, and in a second direction opposite the first direction through the feeding set.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/00 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 31/00 - Dispositifs pour l'introduction ou la rétention d'agents, p. ex. de remèdes, dans les cavités du corps
A flow control apparatus comprising a housing capable of receiving a portion of the feeding set, a pumping device configured to receive the feeding set and may produce a fluid flow in the feeding set and deliver fluid to a subject, an ultrasonic sensor may be configured to produce a sensor signal indicative of a condition of the feeding set, and a control circuit in communication with the ultrasonic sensor for receiving the sensor signal from the ultrasonic sensor indicative of the condition of the feeding set. The ultrasonic sensor may comprise a plurality of sensor components which may be configured to emit an ultrasonic signal in a first direction, and in a second direction opposite the first direction through the feeding set.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/00 - Dispositifs pour faire pénétrer des agents dans le corps par introduction sous-cutanée, intravasculaire ou intramusculaireAccessoires à cet effet, p. ex. dispositifs de remplissage ou de nettoyage, appuis-bras
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 31/00 - Dispositifs pour l'introduction ou la rétention d'agents, p. ex. de remèdes, dans les cavités du corps
57.
System, method, and device utilizing reversible connector
A compression garment that is selectively engageable and operable by a controller for inflation via a reversible connector, the compression garment comprising a plurality of bladders and compression garment tubing. The compression garment tubing includes a plurality of garment tubes in fluid communication with the plurality of bladders at a first compression garment tubing end and includes a second compression garment tubing end opposite the first compression garment tubing end. The reversible connector has a first connector portion and second connector portion, the first connector portion and the second connector portion being selectively reversibly connectable together to form the reversible connector.
F16L 37/56 - Accouplements du type à action rapide pour tuyaux à double-paroi ou à canaux multiples
F16L 39/00 - Raccords ou accessoires de raccordement pour tuyaux à double paroi ou à canaux multiples ou pour assemblages de tuyaux
F16L 39/02 - Raccords ou accessoires de raccordement pour tuyaux à double paroi ou à canaux multiples ou pour assemblages de tuyaux pour manches
F16L 37/12 - Accouplements du type à action rapide dans lesquels l'assemblage entre les extrémités s'aboutant ou se chevauchant est maintenu par des organes de blocage utilisant des crochets, cliquet, ou autres organes de blocage mobiles ou que l'on peut insérer
58.
SYSTEM, METHOD, AND DEVICE UTILIZING REVERSIBLE CONNECTOR
A compression garment that is selectively engageable and operable by a controller for inflation via a reversible connector, the compression garment comprising a plurality of bladders and compression garment tubing. The compression garment tubing includes a plurality of garment tubes in fluid communication with the plurality of bladders at a first compression garment tubing end and includes a second compression garment tubing end opposite the first compression garment tubing end. The reversible connector has a first connector portion and second connector portion, the first connector portion and the second connector portion being selectively reversibly connectable together to form the reversible connector.
The present disclosure provides a device for holding at least one conduit. The device includes a ring having a first end, a second end, a first clamping jaw and a second clamping jaw extending from the first end. A first clamping surface of the first jaw contacts a second clamping surface of the second jaw in a first position, and the first clamping surface is spaced apart from the second clamping surface in a second position. The device also includes a channel including an inlet positioned at the second end of the ring. The channel is configured to releasably receive the at least one conduit via the inlet, and the channel prevents the at least one conduit from contacting the first end of the ring.
A61M 1/02 - Appareils pour transfusion sanguine d'un corps à un autre
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
The present disclosure provides a device for holding at least one conduit. The device includes a ring having a first end, a second end, a first clamping jaw and a second clamping jaw extending from the first end. A first clamping surface of the first jaw contacts a second clamping surface of the second jaw in a first position, and the first clamping surface is spaced apart from the second clamping surface in a second position. The device also includes a channel including an inlet positioned at the second end of the ring. The channel is configured to releasably receive the at least one conduit via the inlet, and the channel prevents the at least one conduit from contacting the first end of the ring.
A61M 1/02 - Appareils pour transfusion sanguine d'un corps à un autre
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
The present disclosure provides a device for holding at least one conduit. The device includes a ring having a first end and a second end. The device also includes a first clamping jaw extending from the first end of the ring. The device also includes a second clamping jaw extending from the first end of the ring. A first clamping surface of the first jaw contacts a second clamping surface of the second jaw in a first position, and the first clamping surface is spaced apart from the second clamping surface in a second position. The device transitions from the first position to the second position in response to application of an external force applied to an exterior surface of the ring between the first end and the second end. The device also includes a channel including an inlet positioned at the second end of the ring. The channel is configured to releasably receive the at least one conduit via the inlet, and the channel prevents the at least one conduit from contacting the first end of the ring.
An apparatus and method for delivering fluid from a syringe to a subject using a pumping device of a flow control apparatus. The method includes locating the flow control apparatus on a horizontal support surface. Providing the syringe with a volume of fluid including a total amount of preferred nutrient and an amount of non-preferred nutrient liquid. Mounting the syringe relative to the flow control apparatus whereby the syringe is oriented in a generally vertical orientation such that an outlet of the syringe faces upward. Initiating operation of the pumping device to draw the fluid from the syringe for a duration of time to preferentially deliver at least a portion of the total amount of preferred nutrient in the fluid to the subject.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/145 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons
An apparatus and method for delivering fluid from a syringe to a subject using a pumping device of a flow control apparatus. The method includes locating the flow control apparatus on a horizontal support surface. Providing the syringe with a volume of fluid including a total amount of preferred nutrient and an amount of non-preferred nutrient liquid. Mounting the syringe relative to the flow control apparatus whereby the syringe is oriented in a generally vertical orientation such that an outlet of the syringe faces upward. Initiating operation of the pumping device to draw the fluid from the syringe for a duration of time to preferentially deliver at least a portion of the total amount of preferred nutrient in the fluid to the subject.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61J 1/05 - Récipients spécialement adaptés à des fins médicales ou pharmaceutiques pour recueillir, stocker ou administrer du sang, du plasma ou des liquides à usage médical
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
An apparatus and method for delivering fluid from a syringe to a subject using a pumping device of a flow control apparatus. The method includes locating the flow control apparatus on a horizontal support surface. Providing the syringe with a volume of fluid including a total amount of preferred nutrient and an amount of non-preferred nutrient liquid. Mounting the syringe relative to the flow control apparatus whereby the syringe is oriented in a generally vertical orientation such that an outlet of the syringe faces upward. Initiating operation of the pumping device to draw the fluid from the syringe for a duration of time to preferentially deliver at least a portion of the total amount of preferred nutrient in the fluid to the subject.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61M 5/14 - Dispositifs de perfusion, p. ex. perfusion par gravitéPerfusion sanguineAccessoires à cet effet
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61J 1/05 - Récipients spécialement adaptés à des fins médicales ou pharmaceutiques pour recueillir, stocker ou administrer du sang, du plasma ou des liquides à usage médical
A method of operating an enteral feeding pump to deliver fluid through a pump set, the method comprising determining with a controller of the enteral feeding pump if an occlusion exists in the pump set based on the controller monitoring a sensor signal from a sensor indicative of a rotational position of a rotor of the pump during operation of a motor of the pump to rotate the rotor at a reduced output less than a feeding output for rotating the rotor to produce fluid flow in the pump set during a feeding cycle, the motor operating at the reduced output for a shorter period of time than the feeding output.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
F04B 43/12 - "Machines", pompes ou installations de pompage ayant des organes de travail flexibles à action péristaltique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A cassette for use with a pumping apparatus having a pumping system for engaging a pump set includes a cassette body configured for releasable attachment to the pumping apparatus to mount the cassette on the pumping apparatus. The cassette body has at least one mounting formation. At least one identification member is mounted on the cassette body by the mounting formation of the cassette body. The identification member and mounting formation are formed to mount the identification member in any one of a plurality of predetermined orientations. Each predetermined orientation indicates a different functional configuration of the pump set.
A cassette for use with a pumping apparatus having a pumping system for engaging a pump set includes a cassette body configured for releasable attachment to the pumping apparatus to mount the cassette on the pumping apparatus. The cassette body has at least one mounting formation. At least one identification member is mounted on the cassette body by the mounting formation of the cassette body. The identification member and mounting formation are formed to mount the identification member in any one of a plurality of predetermined orientations. Each predetermined orientation indicates a different functional configuration of the pump set.
A cassette for use with a pumping apparatus having a pumping system for engaging a pump set includes a cassette body configured for releasable attachment to the pumping apparatus to mount the cassette on the pumping apparatus. The cassette body has at least one mounting formation. At least one identification member is mounted on the cassette body by the mounting formation of the cassette body. The identification member and mounting formation are formed to mount the identification member in any one of a plurality of predetermined orientations. Each predetermined orientation indicates a different functional configuration of the pump set.
A pump set for use with a pumping apparatus to deliver nutrition to an infant includes a first container to receive breast milk; a second container to receive fortifier; tubing extending from the first container and from the second container; and a valve mechanism connected to the first and second containers by the tubing and configured to selectively pass liquid from the first container and the second container.
A pump set for use with a pumping apparatus includes tubing for carrying a liquid. A valve mechanism is mounted to the tubing between an inlet section and a pump engagement section. The valve mechanism includes a first port connected to the inlet section of the tubing, a second port connected to the pump engagement section of the tubing, and a valve disposed between the first and second ports. The valve includes a stem rotatably mounted within a stem holder. The stem includes a flow passage extending through the stem and having an open V shape whereby a narrow open end of the flow passage communicates with the first port and a wide open end of the flow passage communicates with the second port to place the inlet section of the tubing in communication with the pump engagement section of the tubing.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A pump set for use with a pumping apparatus includes tubing for carrying a liquid. A valve mechanism is mounted to the tubing between an inlet section and a pump engagement section. The valve mechanism includes a first port connected to the inlet section of the tubing, a second port connected to the pump engagement section of the tubing, and a valve disposed between the first and second ports. The valve includes a stem rotatably mounted within a stem holder. The stem includes a flow passage extending through the stem and having an open V shape whereby a narrow open end of the flow passage communicates with the first port and a wide open end of the flow passage communicates with the second port to place the inlet section of the tubing in communication with the pump engagement section of the tubing.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A61J 15/00 - Tubes pour l'alimentation thérapeutique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A pump set for use with a pumping apparatus includes tubing for carrying a liquid. A valve mechanism is mounted to the tubing between an inlet section and a pump engagement section. The valve mechanism includes a first port connected to the inlet section of the tubing, a second port connected to the pump engagement section of the tubing, and a valve disposed between the first and second ports. The valve includes a stem rotatably mounted within a stem holder. The stem includes a flow passage extending through the stem and having an open V shape whereby a narrow open end of the flow passage communicates with the first port and a wide open end of the flow passage communicates with the second port to place the inlet section of the tubing in communication with the pump engagement section of the tubing.
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
An adapter assembly includes a tapered connector including a central passage and a tapered outer surface for sealing with a tube or bottle. A male connector for connection to a female connector to fluidly communicate the female connector with the tube or bottle is coupled with the tapered connector. A method of forming such an adapter assembly is also disclosed.
A connector system is configured to fluidly connect a nasogastric tube assembly including a lumen and a tube to a medical device. The system includes a connector including: a fitting configured to provide a fluid-tight connection with the medical device; a neck coupled to the fitting, the neck configured to attach to the nasogastric tube assembly; and a body coupled to the neck, the body configured to provide a fluid-tight connection with the nasogastric tube assembly when at least partially inserted within the lumen; and a first tether including a first fastening region defining a first opening configured to receive the neck, a second fastening region defining a second opening configured to couple to the nasogastric tube assembly, and a link coupling the first fastening region to the second fastening region, the link configured to maintain a fixed distance separating the first fastening region from the second fastening region.
The present disclosure provides articles having an absorbent core with a plurality of segmented volumes defined by a network of filaments, with an absorbent material therein. Suitable articles which may be formed with this absorbent core include, for example, diapers such as infant diapers, juvenile diapers and training pants, feminine hygiene products such as menstrual pads, adult incontinence products such as adult briefs, protective underwear, pads and bladder control pads, pet training pads, and other disposable products utilized to absorb fluids.
A61L 15/20 - Bandages, pansements ou garnitures absorbant les fluides physiologiques tels que l'urine, le sang, p. ex. serviettes hygiéniques, tampons contenant des matériaux organiques
A61F 13/539 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant caractérisées par la liaison des couches absorbantes entre elles ou avec les couches extérieures
A61F 13/534 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant ayant une composition non homogène sur toute l'épaisseur du noyau absorbant
A61F 13/535 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant ayant une composition non homogène sur toute l'épaisseur du noyau absorbant non homogène dans le plan de la garniture absorbante, p. ex. les couches absorbantes du noyau étant de différentes tailles
A61F 13/53 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant
A61L 15/24 - Composés macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneLeurs dérivés
A pump set for use with a pumping apparatus having a rotor with a plurality of rollers mounted on the rotor rotatable about an axis of rotation is disclosed. The pump set comprises a cassette body comprising a stator member with a fixed portion secured to the cassette body, a second portion opposite the fixed portion, a reaction surface and a second surface opposite the reaction surface, the reaction surface defined between the fixed portion and the second portion, and a tube secured to the cassette body, at least a portion of the tube is disposed against the reaction surface.
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
F04B 43/12 - "Machines", pompes ou installations de pompage ayant des organes de travail flexibles à action péristaltique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
F04B 43/00 - "Machines", pompes ou installations de pompage ayant des organes de travail flexibles
F04B 43/08 - "Machines", pompes ou installations de pompage ayant des organes de travail flexibles ayant des organes flexibles tubulaires
A flow control apparatus adapted for a feeding set includes a housing capable of receiving at least a portion of the feeding set and a pumping device for acting on the feeding set to produce fluid flow in the feeding set for delivery of fluid. The apparatus has a sensor arranged with respect to the pumping device to produce a signal indicative of a rotational position of a rotor, and a control circuit in communication with the sensor for receiving the sensor signal from the sensor indicative of the rotational position of the rotor and in communication with the pumping device to control operation thereof. The control circuit controls operation of a motor at a first output to rotate the rotor to produce fluid flow in the feeding set and at a second output effectively less than the first output.
A61J 15/00 - Tubes pour l'alimentation thérapeutique
F04B 43/12 - "Machines", pompes ou installations de pompage ayant des organes de travail flexibles à action péristaltique
A61M 5/168 - Moyens pour commander l'écoulement des agents vers le corps ou pour doser les agents à introduire dans le corps, p. ex. compteurs de goutte-à-goutte
A61M 5/142 - Perfusion sous pression, p. ex. utilisant des pompes
A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.
A61F 13/84 - Accessoires, non prévus ailleurs, pour garnitures absorbantes
A61L 15/46 - Désodorisants ou produits pour neutraliser les mauvaises odeurs, p. ex. pour inhiber la formation d'ammoniac ou la multiplication de bactéries
89.
MONITORING VITAL PARAMETERS OF A COMPRESSION GARMENT WEARER
Monitoring vital parameters of a wearer of a compression garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Analyzing the pressure signal waveform for an oscillating amplitude as a function of time and/or a representation of a pulse of the wearer provides an indication of blood pressure of the wearer.
Monitoring vital parameters of a wearer of a compression garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Analyzing the pressure signal waveform for an oscillating amplitude as a function of time and/or a representation of a pulse of the wearer provides an indication of blood pressure of the wearer.
A61B 5/022 - Mesure de la pression dans le cœur ou dans les vaisseaux sanguins par application d'une pression pour fermer les vaisseaux sanguins, p. ex. contre la peauOphtalmodynamomètres
A61B 5/025 - Mesure du pouls ou des pulsations cardiaques utilisant des capteurs engendrant des signaux électriques à l'intérieur de dispositifs d'occlusion, p. ex. en réponse à des bruits de Korotkoff
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
Monitoring vital parameters of a wearer of a compression garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Analyzing the pressure signal waveform for an oscillating amplitude as a function of time and/or a representation of a pulse of the wearer provides an indication of blood pressure of the wearer.
An absorbent article includes a fluid pervious top sheet, a fluid impervious bottom sheet, and an absorbent core positioned therebetween. The top sheet comprises a plurality of bicomponent fibers having target friction characteristics.
A61F 13/53 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant
A61F 13/15 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons
A61F 13/511 - Feuille supérieure, c.-à-d. revêtement ou couche perméable dirigée vers la peau
In one example, a sensor system of a patient monitoring system includes a voiding sensor that includes an electrical circuit configured to be transitioned from a first impedance state to a second impedance state in response to a voiding event in an absorbent region of an absorbent article worn by a patient. The sensor system also includes one or more processors configured to: determine, based on whether the impedance state of the electrical circuit is open or closed, that the voiding event has occurred; and generate, based at least in part on the occurrence of the voiding event, patient status data of the patient. The sensor system also includes a communication module configured to wirelessly transmit, via a relay module, the patient status data to a remote monitoring device that is distinct from the relay module.
G08B 21/00 - Alarmes réagissant à une seule condition particulière, indésirable ou anormale, et non prévues ailleurs
A61F 13/42 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons avec un indicateur ou une alarme d'humidité
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
An absorbent article includes a fluid pervious top sheet, a fluid impervious bottom sheet, and an absorbent core positioned therebetween. The top sheet comprises a plurality of bicomponent fibers having target friction characteristics.
A61F 13/15 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons
A61F 13/20 - Tampons, p. ex. tampons cataméniauxLeurs accessoires
A61F 13/53 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons caractérisées par le milieu absorbant
96.
Connector for connecting a syringe to a gastronomy tube
A connector (10) for connecting a syringe to a gastrostomy tube (12), the connector (10) comprises a bayonet style locking member (16) with a locking projection (40) for locking the connector (10) to the gastrostomy tube (12). The locking projection (40) forms a receiving recess (42) for receiving and locking at least one wing (70) of an end portion (56) of the gastrostomy tube (12). Further, the invention relates to a connector assembly having such a connector (10) and to a method for connecting a syringe to a gastrostomy tube (12).
