A coupling for use in a system (2) for communicating a flow of gas from a pressure generating device (4) to an airway of a patient includes a first portion (16, 16, 16) adapted to be coupled in fluid communication with the pressure generating device and a second portion (10) selectively coupled to the first portion. The second portion is adapted to be coupled in fluid communication with the airway of the patient. At least one of the first portion and the second portion includes an illuminated portion (18, 20), the illuminated portion being adapted to be visible to a patient when the first and second portions are uncoupled and adapted to be not visible to a user when the first and second portions are coupled. The illuminated portion assists a user in locating and recoupling the first and second portions of the coupling in a darkened room.

A connecting structure for medical use includes a first connecting portion 1 and a second connecting portion 2. The first connecting portion 1 includes a threadedly engageable portion 22a, a support portion 22b and a sealing portion 14. The second connecting portion 2 includes a threadedly engageable portion 2c and a sealing portion 2b. The threadedly engageable portions are threadedly engageable with each other. The sealing portions are joinable to each other by advancement of a threaded engagement between the threadedly engageable portions. An operating cylinder 30 is mounted on an outer periphery of the support portion 22b. A torque limiting mechanism 40 is disposed between the operating cylinder 30 and the support portion 22b. The sealing portions 14, 2b can be joined by turning the operating cylinder 30 in a threaded engagement advancing direction. When a rotary torque applied to the operating cylinder 30 reaches a predetermined torque as a result of a resistance generated by the joining of the sealing portions, the operating cylinder 30 is turned free from the support portion 22b. By this arrangement, appropriate sealing properties can be secured and the sealing portions can be prevented from breakages.

A medical connector includes a body having a distal end, a proximal end, and a sidewall extending between the distal end and the proximal end, a helical thread extending radially outward from a surface of the sidewall and comprising a crest portion, flank portions, and a root portion with the flank portions connecting the root portion to the crest portion, and at least one micro-thread extending radially outward from the surface of the sidewall. At least a portion of the micro-thread is spaced apart from the helical thread.

A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. The reservoir, a base and a cap are connected to form an integrated unit that is capable of being inserted and secured in an infusion pump housing. The cap and the infusion pump are each provided with at least one sensor or at least one detectable feature, arranged to interact with at least one corresponding detectable feature or sensor on the other of the cap and infusion pump device, to detect one or more of the presence, position or other characteristic of the cap when the cap is aligned or coupled with the infusion pump housing. The detectable feature and sensor may be magnetic, RF, mechanical, optical or any combination.

A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. The reservoir, a base and a cap are connected to form an integrated unit that is capable of being inserted and secured in an infusion pump housing. The cap and the infusion pump are each provided with at least one sensor or at least one detectable feature, arranged to interact with at least one corresponding detectable feature or sensor on the other of the cap and infusion pump device, to detect one or more of the presence, position or other characteristic of the cap when the cap is aligned or coupled with the infusion pump housing. The detectable feature and sensor may be magnetic, RF, mechanical, optical or any combination.

Disclosed herein are embodiments of a connector system for releasably connecting together tubes, for example medical tubing, and methods of making and using such a connector system, whereby the connector system includes a female coupler having a first passageway, a male coupler having a second passageway, a catch movably coupled to the female coupler, and a catch-receiving element coupled to the male coupler. The connector system further includes a release element movably coupled to the female coupler, whereby travel of the release element along or over a female coupler outer surface of the female coupler disengages the catch from the catch-receiving element to achieve a disconnected condition of the connector system. Further disclosed herein are embodiments of a connector system for releasably connecting together tubes, whereby the connector system includes at least one valve biased by a valve-biasing member disposed external to or outside of the fluid flow path.

A single step body insertion device comprises a cannula and a Veress needle which penetrates the skin surface and relevant tissue layers to reach fluid and/or gases that need to be removed from the body. The cannula shaft and tapered tip are of a polymeric material which is flexible and kink resistant. The Veress needle has an engagement feature for engagement with the tapered tip of the cannula for delivery of the cannula into the body as the Veress needle is inserted into the body. The device is used for the management of conditions such as pneumothoraxes and pleural effusions as well as other conditions that require release of fluid and/or gas from the body.

A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. The reservoir, a base and a cap are connected to form an integrated unit that is capable of being inserted and secured in an infusion pump housing. The cap and the infusion pump are each provided with at least one sensor or at least one detectable feature, arranged to interact with at least one corresponding detectable feature or sensor on the other of the cap and infusion pump device, to detect one or more of the presence, position or other characteristic of the cap when the cap is aligned or coupled with the infusion pump housing. The detectable feature and sensor may be magnetic, RF, mechanical, optical or any combination.

Percutaneous access apparatus is described that comprises a percutaneous fluid access device having an extracorporeal portion, one or more ports accessible from the extracorporeal portion and a septum for sealing each port. A connector device comprising one or more hollow needles is attachable to the percutaneous fluid access device. The apparatus also includes an attachment mechanism for attaching the connector device to the extracorporeal portion and an actuation mechanism that, after the connector device has been attached to the extracorporeal portion, can be used to drive the one or more hollow needles through the septum to establish fluid communication between the one or more hollow needles and the one or more ports. The apparatus may be used for neurosurgery applications.

This invention relates to new apparatuses for draining material from a stomach and infusing fluid into the stomach comprising a tubing connector, a housing unit, and a one-way valve. In an embodiment the connector can have a first port, a second port, a third port and a branched lumen that extends through each of the first, second and third ports. The housing unit can have a housing lumen that is sized and shaped to receive the third port and the housing unit is sized and shaped to receive the connector. The one-way valve can be sized and shaped to be received in the housing lumen.