A medical device includes a multi-layer body defining an interior space configured to contain a liquid. The multi-layer body includes a solid outer wall having a positive Poisson's ratio and a porous inner wall having a negative Poisson's ratio. A method of making a multi-layer body includes applying a stimulus to a precursor material to cause the precursor material to form a porous wall having a negative Poisson's ratio, and attaching a solid wall to the porous wall to form the multi-layer body, the solid wall having a positive Poisson's ratio. A suture includes one or more filaments, at least a first filament of the one or more filaments including a negative Poisson's ratio material. A medical device includes a biocompatible hydrogel, and the biocompatible hydrogel includes a composite of a first material having a negative Poisson's ratio and a second material having a positive Poisson's ratio.

A medical device includes a multi-layer body defining an interior space configured to contain a liquid. The multi-layer body includes a solid outer wall having a positive Poisson's ratio and a porous inner wall having a negative Poisson's ratio. A method of making a multi-layer body includes applying a stimulus to a precursor material to cause the precursor material to form a porous wall having a negative Poisson's ratio, and attaching a solid wall to the porous wall to form the multi-layer body, the solid wall having a positive Poisson's ratio. A suture includes one or more filaments, at least a first filament of the one or more filaments including a negative Poisson's ratio material. A medical device includes a biocompatible hydrogel, and the biocompatible hydrogel includes a composite of a first material having a negative Poisson's ratio and a second material having a positive Poisson's ratio.

A tube connection part adapted to accommodate a flexible tube made from a material comprising polyvinyl chloride, wherein said tube connection part comprises a sleeve adapted to form an overlapping region between said tube connection part and said tube, wherein an adhesion promoting agent is deposited on at least a subsection of a surface of said sleeve, characterized in that the adhesion promoting agent comprises a styrene-butadiene block copolymer.

Provided is an ophthalmic instrument that is for retaining a tube member for providing communication between the inside and the outside of an eyeball, such that the tube member is stuck into an outer membrane of the eyeball and that is suitable for retaining the tube member at an outer peripheral portion of a cornea. An ophthalmic instrument includes a main body and a needle portion connected to the main body. The main body has a straight portion and a bent portion. When attaching a tube member to an eyeball, first, the needle portion is inserted through the tube member, and the tube member is stuck into an outer peripheral portion of a cornea as the outer membrane of the eyeball while a hole is made in the outer peripheral portion of the cornea with the needle portion.

A cleanable respiratory tube is provided. The cleanable respiratory tube comprises a corrugated tube adapted for conveying gases to and/or from a patient. The corrugated tube has a first and a second fitting at a first and a second end thereof, respectively. A sheath having a smooth cleanable outer surface encases the corrugated tube. A first and a second end of the sheath is fixedly attached to the respective first and second fitting. The sheath is made of a flexible foil-type sheet material surrounding the corrugated tube having an inside diameter approximately equal to an outside diameter of ridges of the corrugated tube such that the sheath is in a touching relationship therewith.

A wearable infusion pump assembly. The wearable infusion pump assembly includes a reservoir for receiving an infusible fluid and a fluid delivery system configured to deliver the infusible fluid from the reservoir to an external infusion set. The fluid delivery system includes a controller, a pump assembly for extracting a quantity of infusible fluid from the reservoir and providing the quantity of infusible fluid to the external infusion set, the pump assembly comprising a pump plunger, the pump plunger having distance of travel, the distance of travel having a starting position and an ending position, at least one optical sensor assembly for sensing the starting position and ending position of the pump plunger distance of travel and sending sensor output to the controller, and a first valve assembly configured to selectively isolate the pump assembly from the reservoir, wherein the controller receives the sensor output and determines the total displacement of the pump plunger.

A wearable infusion pump assembly. The wearable infusion pump assembly includes a reservoir for receiving an infusible fluid and a fluid delivery system configured to deliver the infusible fluid from the reservoir to an external infusion set. The fluid delivery system includes a controller, a pump assembly for extracting a quantity of infusible fluid from the reservoir and providing the quantity of infusible fluid to the external infusion set, the pump assembly comprising a pump plunger, the pump plunger having distance of travel, the distance of travel having a starting position and an ending position, at least one optical sensor assembly for sensing the starting position and ending position of the pump plunger distance of travel and sending sensor output to the controller, and a first valve assembly configured to selectively isolate the pump assembly from the reservoir, wherein the controller receives the sensor output and determines the total displacement of the pump plunger.

An infusion base for attachment to a user of an infusion set comprises an adapter having a lower portion, an inner wall portion, and a gap between the lower portion and the inner wall portion. At least one of the lower portion and the inner wall portion is configured to receive an attachment.

Tubing retention systems are described herein. A tubing retention system includes a spigot, a tubing, and a collar. The spigot includes a spigot body and a spigot extension extending from the spigot body, wherein the spigot extension comprises a flared portion opposite to the spigot body and the spigot body and the spigot extension cooperatively define a spigot lumen. The tubing includes an outer surface and a tubing lumen, wherein a coupling portion of the tubing is disposed around the spigot extension, permitting fluid communication between the tubing lumen and the spigot lumen. The collar is disposed radially around the outer surface of the tubing and axially between the flared portion and the spigot body, wherein the collar radially engages the coupling portion of the tubing disposed around the spigot extension to axially and radially retain the tubing with the spigot.

A device and method for holding coils of medical tubing is provided to simplify packaging and organizing the various coils of medical tubing needed for a medical device. This will make it easier for the patient to manipulate each coil of tubing, particularly in a home setting involving a home dialysis machine operated by the patient. The tube holding device advantageously reduces the probability of entanglement and groups the coils of tubing individually. It also mitigates and/or eliminates the need for tape to bundle the coils. Specifically, benefits of the tube holding device according to the system described herein include: reduced cost; ease-of-use; prevention of entanglement of coils of tubing; ease of packaging and shipping; and does not require packaging tape to bundle tubing.