Disclosed is a method for manufacturing a cannula unit with a cannula housing and a cannula, in which a cannula is injection molded onto a molding core pin having an outer diameter d1 to produce a cannula having a distal end with a larger outer diameter than the outer diameter of the remaining cannula, a first distal section adjoining the distal end, a second proximal section adjoining the first distal section, and a proximal end. A cannula housing is injection molded onto the distal end and the first distal section of the cannula and the molding core pin is removed from the cannula. A piercing needle with an outer diameter d4 is threaded into the cannula, wherein the diameter d4 of the piercing needle is chosen such that it is smaller than the diameter d1 of the molding core pin.

A method of manufacturing a medical device, including forming a flexible base portion to have a plurality of through-holes therethrough, placing the flexible base portion on a non-patient side of an adhesive patch with the through-holes in communication with the adhesive patch, dispensing an adhesive into the through-holes onto the adhesive patch and walls of the flexible base portion surrounding the through-holes; and curing the adhesive to form an adhesive plug mechanically bonding the flexible base portion to the adhesive patch.

A polymeric device including: an elongated hollow tube having an outer surface; and a spiral fin wound around the outer surface of the hollow tube; wherein the hollow tube and the spiral fin are formed of a single unitary piece through a molding process. The polymeric device can further include a longitudinal projection projecting from the outer surface of the hollow tube, the longitudinal projection having a greater thickness than other portions of the hollow tube and the longitudinal projection extending at least a portion of a longitudinal length of the hollow tube.

An implantable medical device is described. The implantable medical device includes an anti-condensation filler that is highly permeable to a predetermined class of small molecules, such as oxygen. The implantable medical device includes a small molecule discharge bag that is permeable to the small molecule, and a cannula that connects an interior of the small discharge bag to the anti-condensation filler. In operation, small molecules are collected and transported through the anti-condensation filler to the cannula for diffusion through the small molecule discharge bag. Even when this device is implanted in a high humidity and temperature gradient environment, the anti-condensation filler prevents condensation, such as water condensation.

A cannula assembly having a retention member and a method of manufacture of the cannula assembly is provided. The cannula assembly includes a cannula and a sleeve disposed around the cannula from a proximal end to a distal end. The sleeve can be pre-formed by a stretch blow molding process then advanced over the cannula. The sleeve includes an inflatable balloon and an annular ring distal the inflatable balloon. The cannula includes an annular recess. The annular ring is sized to have an interference fit with the annular recess.

Disclosed is a method for manufacturing a cannula unit with a cannula housing and a cannula, in which a cannula is injection molded onto a molding core pin having an outer diameter d1 to produce a cannula having a distal end with a larger outer diameter than the outer diameter of the remaining cannula, a first distal section adjoining the distal end, a second proximal section adjoining the first distal section, and a proximal end. A cannula housing is injection molded onto the distal end and the first distal section of the cannula and the molding core pin is removed from the cannula. A piercing needle with an outer diameter d4 is threaded into the cannula, wherein the diameter d4 of the piercing needle is chosen such that it is smaller than the diameter d1 of the molding core pin.

A cannula assembly having a retention member and a method of manufacture of the cannula assembly is provided. The cannula assembly includes a cannula and a sleeve disposed around the cannula from a proximal end to a distal end. The sleeve can be pre-formed by a stretch blow molding process then advanced over the cannula. The sleeve includes an inflatable balloon and an annular ring distal the inflatable balloon. The cannula includes an annular recess. The annular ring is sized to have an interference fit with the annular recess.

An adhesive patch is secured to an infusion set, patch pump or other on-body medical device by an overmolding process during manufacture of the medical device, or during manufacture of a portion of the medical device, without the need for a separate adhesive. This provides a more secure connection between the patch and the medical device, and reduces the required number of adhesive layers from two (skin attachment side and device attachment side) to one (skin attachment side only), thereby simplifying the design and manufacture of the patch.

The invention provides a surgical tool (1), e.g. a hand-held tool, for inserting surgical implants in a patient's body, the tool comprising: a main body (2) extending along a longitudinal axis (X-X) between firstly a working end (3) and secondly a proximal end (4), the main body (2) also presenting an outside surface (5) connecting the working end (3) to the proximal end (4); and a guide cannula (14) arranged within the main body (2) and extending between a distal orifice (15) opening to the outside of said main body (2) at the working end (3), and a rear orifice (16); said surgical tool (1) being characterized in that said rear orifice (16) opens out to the outside surface (5) of said main body (2), and in that said main body (2) presents longitudinal splines (25, 27, 28) projecting from said main body (2) in respective planes extending. radially relative to the longitudinal axis (X-X). Surgical instrumentation.

An implantable medical device is described. The implantable medical device includes an anti-condensation filler that is highly permeable to a predetermined class of small molecules, such as oxygen. The implantable medical device includes a small molecule discharge bag that is permeable to the small molecule, and a cannula that connects an interior of the small discharge bag to the anti-condensation filler. In operation, small molecules are collected and transported through the anti-condensation filler to the cannula for diffusion through the small molecule discharge bag. Even when this device is implanted in a high humidity and temperature gradient environment, the anti-condensation filler prevents condensation, such as water condensation.