A61M39/12

DYNAMICALLY RIGIDIZING COMPOSITE MEDICAL STRUCTURES

A rigidizing device includes a plurality of layers and an inlet between the elongate flexible tube and the outer layer and configured to attach to a source of vacuum or pressure. The rigidizing device is configured to have a rigid configuration when vacuum or pressure is applied through the inlet and a flexible configuration when vacuum or pressure is not applied through the inlet.

STRAIN RELIEF ADAPTER FOR MEDICAL TUBING CONNECTION

A strain relief adapter (100) for a medicament delivery device (200) includes a flexible body (101) having a first end (102) configured to connect to one of a fluid connector and a pump connector, a second end (104) configured to connect to tubing, a hollow fluid path (108, 110, 112, 114) therethrough fluidly connecting the first and second ends, and a plurality of external strain relief ridges (106) disposed between the first and second ends.

SINGLE MONOLITHIC PIECE PIVC-INTEGRATED HEMOLYSIS-REDUCTION ACCESSORIES FOR DIRECT BLOOD DRAW
20230065702 · 2023-03-02 ·

A flow restriction device may include a male luer connector portion, a female luer connector portion disposed proximally to the male luer connector portion, and a body portion extending between the male and female luer portions, and integrally formed with the male and female luer portions to form a single monolithic piece. The male luer connector portion may have an internal surface defining a lumen thereof, and the female luer connector portion may have an internal surface defining a lumen fluidly connected to the lumen of the male luer connector portion. The body portion may have a recess extending longitudinally therethrough and fluidly communicated with the lumens of the male luer portion and the female luer portion. The recess may define a micro-channel along which fluid flows from the male luer connector portion into the fluid collection device via the female luer connector portion.

SINGLE MONOLITHIC PIECE PIVC-INTEGRATED HEMOLYSIS-REDUCTION ACCESSORIES FOR DIRECT BLOOD DRAW
20230065702 · 2023-03-02 ·

A flow restriction device may include a male luer connector portion, a female luer connector portion disposed proximally to the male luer connector portion, and a body portion extending between the male and female luer portions, and integrally formed with the male and female luer portions to form a single monolithic piece. The male luer connector portion may have an internal surface defining a lumen thereof, and the female luer connector portion may have an internal surface defining a lumen fluidly connected to the lumen of the male luer connector portion. The body portion may have a recess extending longitudinally therethrough and fluidly communicated with the lumens of the male luer portion and the female luer portion. The recess may define a micro-channel along which fluid flows from the male luer connector portion into the fluid collection device via the female luer connector portion.

Wound care connection device and wound care kit

The invention relates to a device for connecting multi-lumen lines for the medical field, in particular for wound care in the field of vacuum therapy, having a preferably one-piece basic body, designed for tight and preferably releasable connection of at least two line lumens, wherein the basic body, for furnishing a distributor chamber for at least one, preferably two, three, or more lumens, opening into it, of the connected line and preferably at least one channel for removing a fluid from and introducing it into the distributor chamber, and when the line is connected, the distributor chamber is sealed off in fluid-tight fashion from at least one line lumen in such a way that a fluid exchange between the distributor chamber and this line lumen is prevented.

Wound care connection device and wound care kit

The invention relates to a device for connecting multi-lumen lines for the medical field, in particular for wound care in the field of vacuum therapy, having a preferably one-piece basic body, designed for tight and preferably releasable connection of at least two line lumens, wherein the basic body, for furnishing a distributor chamber for at least one, preferably two, three, or more lumens, opening into it, of the connected line and preferably at least one channel for removing a fluid from and introducing it into the distributor chamber, and when the line is connected, the distributor chamber is sealed off in fluid-tight fashion from at least one line lumen in such a way that a fluid exchange between the distributor chamber and this line lumen is prevented.

INSTRUMENT CONNECTION DEVICE AND METHOD FOR PRODUCTION THEREOF
20230115919 · 2023-04-13 · ·

An instrument connection device having a flexible hose-like body with a flexible wall in which the proximal end of a hose is inserted. The hose has a lumen that extends longitudinally through the hose. A wire is arranged inside the hose, for example, inside the lumen. The wire is guided through a punctured hole in the wall that the wire may create during a penetration of wall. The punctured hole may be straight and guides the obliquely. For example, the hole may be inclined to the radial axis and the longitudinal center axis.

INSTRUMENT CONNECTION DEVICE AND METHOD FOR PRODUCTION THEREOF
20230115919 · 2023-04-13 · ·

An instrument connection device having a flexible hose-like body with a flexible wall in which the proximal end of a hose is inserted. The hose has a lumen that extends longitudinally through the hose. A wire is arranged inside the hose, for example, inside the lumen. The wire is guided through a punctured hole in the wall that the wire may create during a penetration of wall. The punctured hole may be straight and guides the obliquely. For example, the hole may be inclined to the radial axis and the longitudinal center axis.

Devices and methods for vascular hyperperfusion of extravascular space

A method of delivering a therapeutic substance for treatment to a region of the body through vascular isolation and manipulation of fluid flux into and from the region of the body including the steps of: restricting vascular inflow to the region of the body; washing out oncotically active plasma proteins from the region of the body by increasing the outward oncotic pressure gradient from the region of the body; inducing ischemia in the region of the body; controlling the pressure and fluid flow of the main blood vessels to and from the region of the body; providing the therapeutic substance to the region of the body when the fluid flow to the region of the body is controlled.