A drug delivery device may include a cassette with a needle assembly and a cartridge. The cassette is configured to couple and decouple from a reusable module. The device may also comprise an orientation mechanism to orient the cassette in relation to another device, such as a reusable housing. The device may comprise an extendable and retractable needle assembly. The cassette configuration is adapted to have a stopper with a short travel (no more than 14 mm) to deliver 1 mL of medication. The cassette may have a ratio of height to diameter from 2:1 to 1:1. The cassette may include a pair of drivable interfaces for being driven to actuate the stopper to expel medication and to drive the needle assembly between a retracted and extended configuration for controlled fluid communication between the needle and reservoir.

A patch pump includes a needle assembly, a reservoir, a preparation, and an inflatable component. The needle assembly includes a cannula, and a plunger slidably disposed in the cannula. The plunger has a pointed tip and is structured to move within the cannula upon application of a force on the plunger such that the pointed tip of the plunger extends from the cannula to form a channel in a tissue of a subject. The reservoir is fluidically coupled to the needle assembly, and the preparation is contained in the reservoir. The inflatable component is structured to, upon inflation, press against the reservoir to force the preparation from the reservoir and into a flowpath between the reservoir and the cannula.

The invention relates to a device for treating an individual suffering from cardiac or circulatory arrest or from a stroke, comprising a blood withdrawal device (BE) that is applied to the individual (P), an analysis unit (BA) which is directly or indirectly connected to the blood withdrawal device for detecting a blood analysis result (BAE) providing at least one characteristic of the blood, directly or indirectly connected to a blood return device (BR) that is applied to the individual (P) and is designed to deliver a substance to the individual via the return device (BR).

Systems and methods for delivering a medication to a person experiencing an emergency medical event without requiring intervention or action on the part of the person. A device encases a reservoir of medication and a delivery mechanism. Sensors in the housing sense a physical attribute of the person and circuitry monitors information collected by the sensors to determine if the person is experiencing a severe medical condition or event based on the information. An input device on or in the housing, such as a button, may be used or activated by the person if the detected condition or event is a false positive to cancel further action. If the system does not include the button or if the user does not press it in time, the system activates the delivery device and injects the medication into the person.

A method of displaying blood glucose information may include monitoring blood glucose levels of a user, where the blood glucose levels include at least a current blood glucose level and a historic blood glucose level. The method may also include presenting the current blood glucose level using a point indicator along an approximately horizontally centered axis based on a non-linear scale, and presenting the historic blood glucose level and a predicted future blood glucose level on the display as a single smoothed curve passing the point indicator.

An infusion pump device comprises a pump unit having an inlet and an outlet, a connector being in fluid communication with the inlet of said pump unit, a medication reservoir accommodation portion for accommodating a medication reservoir having a label or tag so that an outlet of the medication reservoir is to be coupled to said connector, and a reader which is provided at said medication reservoir accommodation portion so that the reader is adapted to read a label or tag of the medication reservoir when arranged at said medication reservoir accommodation portion.

A peristaltic infusion pump tube segment comprises a first tube portion having a surrounding wall adapted for an upstream occlusion detection, a second tube portion downstream of said first tube portion and adapted to be temporally engaged by an engagement structure, wherein said second tube portion comprises a surrounding wall being at least partly thicker than the wall of said first tube portion and made of an elastic material which allows said second tube portion to be essentially reformed at those portions which are currently not subject to the engagement by the engagement structure, a third tube portion downstream of said second tube portion and having a surrounding wall adapted for an air in line detection, and a fourth tube portion adapted for a downstream pressure detection. The peristaltic infusion pump tube segment is provided in an infusion pump device which comprises a pump mechanism configured as a peristaltic mechanism.

Medical devices and related patient management systems and methods are provided. A method of monitoring a plurality of patients involves a computing device obtaining measurement data for the plurality of patients from a database, obtaining one or more prioritization rules from the database, generating a prioritized list of the plurality of patients based on the measurement data in accordance with the one or more prioritization rules, and providing a dashboard graphical user interface (GUI) display including the prioritized list. The prioritized list on the dashboard GUI display is dynamically updated in accordance with the prioritization rule(s) in response to updated measurement data in the database.

A medication delivery patch that is applied to the skin and activated to deliver a medication or other fluid into or through the skin. The patch may be completely mechanically driven, with no electronic components, for low cost, safety, and reliability. Pressing an activation button may set in motion a sequence of mechanical events that result in a needle exiting the patch into the skin of the user, and flow of fluid from an internal pouch in the patch into the user. When delivery is complete, another sequence of mechanical events may occur to retract the needle from the skin and stop the flow of fluid, and to show a visible indicator that delivery is complete. The patch may contain a fluid channel, such as a microfluidic channel, that controls the rate and time of delivery; this channel can be configured or selected for different medications or use cases.

An example agent administration device may comprise a housing. The device may further comprise a sharp assembly including a delivery sharp. The sharp assembly may be reciprocally displaceable along a guide channel of the housing. The device may further comprise an access port in fluid communication with the delivery sharp. The device may further comprise an actuation assembly configured drive the sharp assembly, via urging of a single bias member, from a storage state in which the delivery sharp is within the housing, through a first extended position in which the delivery sharp extends a maximum distance from the housing and to a partially retracted position in which the delivery sharp extends a lesser distance from the housing.