Abstract: The subject matter disclosed herein provides methods for conducting tests on a medical device. A request to conduct a test on a medical device module remotely located from a party initiating the request can be received. The module can have an inductive receiver and be part of a medical device system having an inductive backplane and multiple mounting seats. Each mounting seat can have an inductive transmitter, and the module can be inductively powered when affixed to a first mounting seat. The test can relate to an attribute of the first mounting seat's inductive transmitter or the module's inductive receiver. The request can identify the module and test to conducted. A message representative of the request can be transmitted to the system. Test data relating to an attribute of the inductive transmitter or inductive receiver can be received and provided. Related methods, apparatus, systems, techniques and articles are also described.

Abstract: A stable flow regulator assembly includes a body having an aperture that received a tube. The assembly also includes a worm gear that extends through, and is rotationally movable relative to, the body. A worm wheel is rotationally positioned within the body and is pivotably moved within the body by engagement with the worm gear. The worm wheel also includes a slot, configured to align with the aperture, through which a tube may be extended, and as the worm wheel is moved within the body, the slot and the aperture are moved out of and into alignment to compress and release compression upon the tube.

Abstract: Fluid connector systems including first and second connector portions couplable together to form a fluid pathway therethrough and can resist separation or permit separation as desired. A connector portion can include a connector housing and a cover portion. The connector housing includes a connector body and an engagement portion. The connector body defines a tubing opening and a mating opening. The connector body defines a flow path between the tubing opening and the mating opening. The engagement portion at least partially surrounds the connector body. The engagement portion defines an engagement lip extending radially toward the connector body and is configured to releasably engage the connector housing. The flow path includes at least one portion that is normal to the engagement portion. Fluid flow through the flow path exerts a normal force on the connector housing and prevent release of the connector housing with the mating connector portion.

Abstract: A system for applying a lavage fluid to a surface, the system having a body configured to house a lavage fluid, an application member in fluid communication with the body, the application member being configured to dispense the lavage fluid, and a warming component configured to communicate with the body so as to transfer energy from the warming component to the body sufficient to warm the lavage fluid housed in the body.

Abstract: A flow control device includes a housing having a primary inlet, a secondary inlet, and an outlet disposed downstream of the primary and secondary inlets. The flow control device further includes a chamber defined by an inner circumferential surface of the housing. The chamber fluidly connects the primary and secondary inlets with the outlet. A valve member is mounted in the chamber to pivot toward and block the primary inlet by fluid pressure in the secondary inlet when fluid pressure into the secondary inlet is higher than fluid pressure into the primary inlet.

Abstract: A medication delivery module is mounted to a patient care device, and a first graphic representative of the first medication delivery module is displayed on a display screen of the device, wherein the first graphic includes an information display area for display of infusion information associated with the first medication delivery module, and a status indicator for display of status information associated with the medication delivery module. Responsive to the indication, the status indicator is dynamically orienting such that the status indicator is displayed on a side of the first graphic nearest the coupling of the first medication delivery module. Infusion information from the first medication delivery module is displayed within the display area of the first graphic.

Abstract: Described is a priming device to prime a gas from a fluid delivery system by receiving the gas and a fluid used to push the gas into a chamber, the priming device including a housing having a chamber, an inlet port, and an opening to release gas received into the chamber. The device further includes a valve extending from the inlet port toward the chamber and a cover body comprising one or more flexible protrusions extending axially inward from an inner surface of the cover body. The cover body has an open first end, an open second end, and an axis between the first end and the second end, the first end configured to couple with a male luer connector, the second end configured to couple with the inlet port of the housing, wherein the cover body is moveable relative to the housing.

Abstract: A flow controller having an internal tubing is provided. The flow controller may include an upper housing having a plurality of graduations, a lower housing engaged with and slidably coupled to the lower housing, and a cavity defined between the upper and lower housings for accommodating at least a portion of internal tubing. The flow controller may further include a flexible clamp having an upper section mounted in the upper housing and a lower section slidably disposed in the lower housing. The upper and lower housings may be slidably coupled relative to each other to transition the internal tubing from (i) an open position where a lumen of the internal tubing is uncompressed by the flexible clamp to (ii) a closed position where the lumen of the tubing is at least partially constricted by the flexible clamp.

Abstract: A reader device is configured to wirelessly read medical information from a medical identification device and location information from a location identification device when the devices are within a range of the at least one reader device. A tracking device receives an indication that first medical information and first location information was read at a first location when a first medical identification device associated with the first medical object and a first location identification device associated with the first location was read at the first location by at least one reader device, and a last-known location of the first medical object associated with the medical identification device is generated based on the first location information read at the first location. In response to receiving a tracking request for a delivery status of a first medical object, the last-known location is provided display responsive to the tracking request.

Abstract: A pumping system comprising a pump comprising a door for access within a housing of the pump, a pump segment configured for conveying a fluid based on compression of the pump segment, a pump segment frame for preventing said pump segment from stretching, a visual placement indicator configured for facilitating in a proper placement of the pump segment frame in the housing, and a non-pinching valve configured to be disposed in the housing and to control a flow of the fluid without requiring pinching of a tube.

Abstract: Syringe assemblies are described herein. A syringe assembly includes an assembly housing, a first syringe, a second syringe, and a connecting gear. The first syringe is disposed within the assembly housing. Each plunger is movable within the respective syringe cavity and defines a respective chamber in the respective syringe cavity, wherein the respective chamber is in fluid communication with the respective syringe port, the respective plunger comprising a respective gear rack extending longitudinally along the respective plunger. The connecting gear is rotatably coupled to the assembly housing. The connecting gear is configured to be in meshed engagement with at least one of the first gear rack and the second gear rack of the syringes.

Abstract: A needleless connector includes a housing having a central longitudinal axis, a body portion, and a base portion. The body portion includes an inner surface forming an internal cavity, and a first port forming a first fluid passage to the housing cavity. The base portion includes a top end section and a bottom end section. The top end section has a protrusion, and the bottom end portion has a second port forming a second fluid passage to the housing cavity. The needleless connector further includes a valve having a wall with an inner surface forming a valve cavity. The valve is coupled with the housing such that the protrusion is positioned in the valve cavity, and a proximal end of the protrusion is spaced apart from a proximal end of the valve cavity.

Abstract: A connector comprises a body having a tubing portion and a luer portion axially opposite the tubing portion and connected thereto, an internal passageway defined by an inner circumferential surface of the connector, the passageway extending axially between the tubing portion and the luer portion and in fluid communication therewith, a stopping mechanism disposed in the luer portion and configured to limit an extent of a fluid line disposed in the connector, and a retaining mechanism disposed in the tubing portion and configured to retain the fluid line in the connector.

Abstract: A method includes receiving a request to activate a medical device. Response to receiving the request, the method includes generating an automatic programming request (APR) for programming the medical device, receiving a message indicating that the APR failed to activate the medical device, and obtaining historical programming records (HPR)s. The method includes determining that parameters in the APR correspond to historical parameters, identifying a set of HPRs including a historical parameter value corresponding to a requested parameter value included the APR, and generating a deviation metric indicating a degree of difference between a secondary parameter value included in the APR and a corresponding historical parameter value. The method includes, responsive to a determination that a deviation metric meets a criticality threshold, changing a drug library record associated with the respective set of deviations and providing an indication to review the changed drug library record.

Abstract: A system for providing aggregated patient data may include a processor and memory. The processor may receive clinical data items from a healthcare data system and device data items from healthcare devices, where the clinical data items and the device data items are associated with patients. The processor may generate patient data objects corresponding to the patients, where each patient data object includes the clinical data items and the device data items associated with one of the patients. The processor may filter the patient data objects based on access privileges of a third party organization to generate filtered patient data objects and transform the filtered patient data objects based on a data transformation rule associated with the third party organization to generate transformed patient data objects. The processor may provide, e.g. over a network, the transformed patient data objects to at least one device associated with the third party organization.

Abstract: An infusion management and monitoring system comprises an infusion pump and instructions executable by a processor to cause a remote device separate from and in communication with the infusion pump to receive data for a medication to be administered to a patient via the infusion pump within a healthcare environment; receive from the infusion pump data for administration of the medication to the patient; determine a status of the administration of the medication based on at least one of the data for the medication or the data for the administration of the medication; and transmit the status to a mobile communication device within the healthcare environment.

Abstract: A system and method for managing inventory in a dispensing cabinet includes a mobile terminal, and an association station configured to associate the mobile terminal with an item type stored in the dispensing cabinet. The association station receives, from the mobile terminal, an indication of a respective item unit of the first item type being moved, determines an access status of one or more containers of the dispensing cabinet when the indication is received, determines a container location for the item unit based on the access status of the containers and receiving the indication of the respective item being moved from the first mobile terminal, and causes, responsive to determining the container location, a supply record associated with the item type and a first container of the dispensing cabinet to be updated to reflect a change to a first amount of the first item type stored in the first container.

Abstract: A disclosed antimicrobial medical device includes a fluid transfer device configured to couple between a patient and a fluid reservoir, a fluid pathway extending through the fluid transfer device, a first electrode coupled to the fluid transfer device, and a second electrode coupled to the fluid transfer device and spaced apart from the first electrode. The first electrode includes a first conductive material and the second electrode includes a second conductive material different from the first conductive material. The second electrode is configured to form a galvanic cell with the first electrode.

Abstract: The disclosed systems and methods manage more notifications between medical devices. A method includes obtaining information corresponding to a clinician and determining whether the information satisfies coordination criteria. The method includes, in accordance with a determination that the clinician is associated with the first medical device and a second medical device, detecting a first and second notification generated by respective medical devices. The method includes identifying, based on detecting the respective notifications, alert information including medical information for a patient receiving medical treatment from the first and second medical device. The method includes determining, based on the identified information, notification priorities between the respective notifications.