The present invention relates to a novel interchangeable lockable catheter having a cap, the cap locking onto a junction hub or base, and encasing at least one lumen proximally to the junction hub of a multi-lumen catheter, PICC line and the like. The interchangeable lockable catheter's cap and base may be made of more than one piece, and provide a locking mechanism sufficient to deter tampering, while providing a low profile, comfortable, sanitary, and efficient means of closing off lumens for patients leaving the treatment area.

A mount provides a structure that facilitates coupling of a nebuliser downstream of a humidifier chamber and upstream of a conduit that delivers conditioned breathing gases to a patient or user. The mount can couple together a chamber, a nebulizer and a conduit.

A medical instrument for endoscopic procedures that is provided with a hollow shaft, such that at least two channels are configured in the shaft and the channels can be coupled on the proximal end with supply conduits. To create a medical instrument of the aforementioned type which is of simple structure and ensures secure connect ability, it is proposed according to the invention that the proximal end of at least one first channel positioned in the shaft and the distal end at least one supply conduit that is to be coupled with this first channel are configured with respect to their geometric structural design in such a way that this first channel and the corresponding supply conduit can be coupled only with one another.

A system for performing an endoscopic surgical procedure in a surgical cavity of a patient that includes a gas delivery device configured to deliver a flow of pressurized gas to a gas delivery lumen extending therefrom, a gaseous sealing module communicating with a distal end of the gas delivery lumen and configured to generate a gaseous seal within a gas sealed lumen extending therefrom, and an access port communicating with a distal end of the gas sealed lumen so as to provide sealed instrument access to the surgical cavity and maintain a stable pressure within the surgical cavity.

An assembly of a dual lumen tubing and a dual bore connector has a first flow conduit along a first lumen and a first bore, and has a second flow conduit from a second bore, via a circumferential groove and along a second lumen. The assembly can be used in connection with an extracorporeal circuit of a haemodialysis machine or an infusion set.

The suction system in the surgical area is part of the operation room, one of its functions is helps to aid the vision of the surgeon and the surgical team. Currently the operation rooms use a regular suction tubing which is just one female connector to the suction system, a body tube and a female connector to the surgical field.

With the modification and adaptation of the regular suction tubing, we will get the new suction tubing in “Y” two-way for surgery, one unit will do the job of 2 regular suction tubing, which will help in saving time to connect, and avoid changing tubes between instruments during the surgery (uncomfortable), less tangles in the surgical field and it will impact in the environment since we will producing fewer PVC which means less material to be disposed.

A catheter assembly includes a catheter, a collar, and an extension tube assembly. The catheter includes a leading end portion and a trailing end portion. The collar is supported on the trailing end portion of the catheter. The extension tube assembly includes a first section and a second section, each section independent of the other section and including a substantially rigid body portion and a compressible extension tube portion. The body portion of each of the first and second sections is independently engageable with the trailing end portion of the catheter. The collar is configured to engage the first and second sections of the extension tube assembly to secure the extension tube assembly to the trailing end portion of the catheter.

Delivery systems and methods for forming and delivering biomaterials from two components are described herein. In particular, apparatus and methods for performing controlled delivery of multicomponent delivery of biomaterials into or onto a body part, such as a body lumen are described. More specifically, in some embodiments, the apparatus and methods are directed towards controlled delivery of micro-volumes of biomaterials into or onto a target location, the micro-volumes being defined as 0.001 mL-1 mL (or 1 μL-1,000 μL) of volume.

A venous reservoir including a single inlet line clamp capable of partially or completely restricting blood flow to the venous reservoir. The venous reservoir is provided with a rigid back plate or bracket that can accommodate an inlet line capable of joining to at least one blood inlet port. The rigid back plate or bracket can accommodate a clamp capable of completely or partially closing the inlet line containing both the cardiotomy line and the venous line to manually control the blood flow drained from the patient.

The invention relates to a An aseptic connector comprising a first connection unit (102; 202; 302; 402; 502) provided with a first terminal end surface (104; 204; 304; 404; 504) and a second connection unit (106; 206; 306; 406; 506) provided with a second terminal end surface (108; 208; 308; 408; 508); said first and second terminal end surfaces are each provided with at least one first and second opening (110, 112; 210, 212; 310, 312; 410, 412; 510, 512), which openings are orientated to substantially coincide when said first and second connection units are connected to each other; said first and second openings are sealed by at least one film (114; 214; 314; 414; 514) arranged on said first and second connection units, so that the contact between the film and each connection unit is aseptic; said at least one film is adapted to be mated with a corresponding film on the other connection unit when said first and second connection units are connected to each other; and said mated films are adapted to be pulled out together two and two after mating such that corresponding first and second openings in said first and second terminal end surfaces are mated aseptically. At least two first ports (116; 216; 316; 416; 516) are arranged on the first connection unit, which first ports have fluid connection with the at least one first opening (110; 210; 310; 410; 510) in the first terminal end surface; and in that at least one second port (118; 218; 318; 418; 518) is arranged on the second connection unit, which the at least one second port has a fluid connection with the at least one second opening (112; 212; 312; 412; 512) in the second terminal end surface.