A catheter package includes an elongated case. A cap is attached to the case by a flexible strap. The case receives the tubing portion of a catheter. The catheter has a funnel attached to the tubing. The funnel has a seal portion releasably engageable with the case. The cap is releasably engageable with the funnel to retain the funnel in contact with the case. A user can flip the cap off the funnel to permit removal of the catheter from the case. The funnel may include ridges or a tactile ring to improve the user's grip on the funnel. An adaptor may be disposed between the funnel and case to allow mating of different cross sectional shapes of the funnel and case. A hydration device may be inserted in the case. Alternately, a tubular liner may be inserted in the case to separate liquid water on the outside of the liner from the catheter tubing on the inside of the liner. A window in the liner mounts a patch of filter material that permits the passage of water vapor into the interior of the liner.

The present invention comprises a compact atomizer that substantially encapsulates a standard inhalant canister and allows for in-line dispensing through a mouthpiece formed in an actuating cover. The compact atomizer comprises an actuating cover and housing that cooperate to secure the canister. By compressing the actuating cover and housing together, a nozzle of the canister is depressed to release a portion of substance within the canister. Compression is enabled by an actuation surface formed in the actuating cover. Substance is released in-line with the canister through a mouthpiece at the end of the actuating cover. The result is a small, compact, yet attractive atomizer that can be carried in a pocket or the like while keeping the canister free of debris.

A medical fluid line connector includes a body defining a central opening extending therethrough, a first projection extending from a first portion of the body, and a second projection extending from a second portion of the body, the second projection being circumferentially and axially offset from the first projection. The first portion of the body and second portion of the body are configured to separate from one another in response to a threshold amount of force being applied to the first projection and the second projection to rotate the first portion of the body and second portion of the body relative to one another.

The invention provides a breast pump system having a belt for wearing by the user of the system. The belt has a pocket for receiving a pump of the system. The pocket has a lateral pocket opening, with a conduit extending from the pump laterally out of the pocket opening. This makes a more comfortable fitting of the pump and easier connection to the expression kit.

Microneedle patches and systems, and methods for use of such patches and systems. In one aspect, a microneedle patch is provided including a tab portion for handling the microneedle patch. In another aspect, a system is provided including a microneedle patch and a tray for housing the microneedle patch. In still another aspect, various indicators providing for providing feedback prior to, during, and after administration of the microneedle patch are provided. Advantageously, the described microneedle patches and systems provide improved handling and ease of application of the microneedle patches to skin for the delivery of therapeutic agents.

The present specification relates to a subassembly for a drug delivery device, the subassembly comprising: a housing adapted to contain a drug container with a needle, a cap, and a spacer, wherein the housing has an inner surface forming a cavity configured to retain the drug container, wherein the cap is configured to be releasably connected to the housing, and wherein the spacer is arranged between the cap and the housing.

A connection unit establishes a fluid connection between a patient and a ventilator. The connection unit includes a patient-side connection piece, a device-side connection piece, a port piece and a central piece, which provides a tube with a curved tube segment and is connected with a fluid-tight connection to the two connection pieces. The port piece includes a straight tube segment and a bent surface with a bent surface and with a passage opening. The port piece is inserted into a receiving opening of the central piece. The bent surface of the port piece forms a part of a wall of the curved tube segment. The straight tube segment of the port piece and the central piece provide a straight tube, which is interrupted by the passage opening. An additional device is insertable through the straight tube segment and through the passage opening into the provided tube.

A patient interface includes: a plenum chamber; a seal-forming structure; a positioning and stabilising structure; a plenum chamber insert configured to be positioned and retained within the plenum chamber; and a vent structure; wherein the plenum chamber insert has a plenum chamber insert port; wherein the plenum chamber insert has an exterior surface configured to be positioned adjacent to an interior surface of the plenum chamber; wherein when the plenum chamber insert is positioned and retained within the plenum chamber, a radial channel is formed by the interior surface of the plenum chamber and the exterior surface of the plenum chamber insert such that gas is able to pass between a patient-proximal side of the plenum chamber insert and a patient-distal side of the plenum chamber insert via the radial channel during use.

A display for outputting information contents of at least one parameter, adjustment value or measurement value of medical devices within at least one display region, wherein the at least one display region is in the form of a tachometer-like display.

A medical system comprising a first device comprising a first handle and a first shaft extending distally from the first handle, wherein the first handle includes a first actuator, a second device comprising a second handle and a second shaft extending distally from the second handle, wherein the second handle includes a second actuator, and a fixture coupling the first device to the second device, wherein a center of the first actuator is within 4.5 inches of a center of the second actuator, and wherein the fixture couples the first device to the second device so that the first handle is configured to be held in a first hand of an operator, while a second hand of the operator traverses between use of the first actuator and the second actuator.