A syringe (1) is provided with a tube (2), a plunger rod (3), and a plunger rod head (4). The plunger rod head (4) has a first surface (41) and a second surface (42). A finger grip component (5) is provided as a one-piece body attached to the tube (2), and includes an injection finger support surface (61) arched in a direction perpendicular to the longitudinal axis (A) with a first curvature for co-operative association with the first surface (41), and an aspiration finger support surface (62) arched in a direction perpendicular to the longitudinal axis (A) with a second curvature for co-operative association with the second surface (42).

A wound care device comprises a cover layer having formed from a stretchable material which has an elastic memory such that upon stretching the first layer will tend to retract to an at-rest position; a layer of adherent on the bottom surface of the cover layer; and a removable release liner removably adhered to the adherent. In use, the wound care device is applied over or adjacent the wound in a stretched/elongated condition extending to be adhered to skin beyond the margins of the wound. The wound care device retracts under its elastic member along lines of tension towards a focal point of lines of tension, thereby drawing the margins of the wound together to stabilize and compress the skin about the wound. The wound care device reduces and absorbs sheer forces directed to the wound that would otherwise disrupt connective tissue of the wound, the device comprising:

A prosthetic device includes a flexible interface configured to conform to a residual limb of a user, a prosthetic socket including an outer shell more rigid than the flexible interface and positioned external to at least a portion of the flexible interface, and one or more vibrational devices placed in connection with the flexible interface to impart vibration to the residual limb.

Drug delivery articles, resident articles, and retrieval systems e.g., for gram-level dosing, are generally provided. In some embodiments, the articles are configured for transesophageal administration, transesophageal retrieval, and/or gastric retention to/in a subject. In certain embodiments, the article includes dimensions configured for transesophageal administration with a gastric resident system. In some cases, the article may be configured to control drug release e.g., with zero-order drug kinetics with no potential for burst release for weeks to months. In some embodiments, the articles described herein comprise biocompatible materials and/or are safe for gastric retention. In certain embodiments, the article includes dimensions configured for transesophageal retrieval. In some cases, the articles described herein may comprise relatively large doses of drug (e.g., greater than or equal to 1 gram).

A safety valve sheet, a breathing tube, a breathing tube assembly and a breathing mask are provided. The safety valve sheet is used for being arranged in the breathing tube which is provided with a safety valve hole of the breathing mask, the safety valve sheet comprises a sheet body, and the sheet body comprises an outer side surface being capable of covering the safety valve hole, wherein a protrusion is formed on the outer side surface, and the protrusion is used for being contacted with an inner side surface of a hole edge of the safety valve hole when the sheet body covers the safety valve hole to form an exhaust gap between the outer side surface and the hole edge. The safety valve sheet is simple in structure and can effectively reduce exhaust noise after being applied to the breathing mask.

A patient interface is configured to deliver a flow of positive pressure respiratory gas to an entrance of a patients airways. The patient interface includes an elastomeric support wall forming at least part of a plenum chamber configured to receive the flow of positive pressure respiratory gas. The patient interface also includes an elastomeric support flange positioned at an end of the elastomeric support wall and extending radially inward from the support wall. The support flange has a flap portion at a central superior region of the support flange that extends further in the radially inward direction than the rest of the support flange. In addition, a foam cushion is mounted on the support flange. The foam cushion is configured to form a seal with the patients face and includes an attachment surface that is in contact with an outer surface of the support flange.

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.

An adhesive convertible tissue stabilizer is provided which can be applied preoperatively to a patient to retract tissue to facilitate a medical/surgical procedure. As a perioperative device, the convertible device accepts most, if not all, surgical preparations, enabling the creation of a sterile field. At the completion of the procedure, the convertible device is converted from a perioperative device to a post-operative device by removal of a layer of the convertible device.

An inventive medical device for transcutaneously inserting a cannula into body tissue. The device has a cannula with a wall that at least partially encloses a lumen. The device also has a patch for mounting onto skin of a user. The patch has a base and has a reservoir for storing a medical fluid. The patch also has a spring driven inserter. The inserter has a drive that urges the cannula from a storage position within the patch to an inserted position within the body tissue. The inserter also has a lock configured for securing the drive in a fixed position. The lock is fixedly connected to the drive and has a snap closure. Also disclosed is a medication pump that is fluidly connectable to the cannula. A method of transcutaneously using the medical device to transcutaneously insert a cannula into body tissue is also disclosed.

A partially deformable impeller has at least two blades, wherein a periphery of each blade is deformable, the periphery being an outermost 5 to 20 percent of a width of the blade. In some embodiments, a catheter blood pump incorporates the partially deformable impeller.