Abstract: The present invention relates generally to medical devices and, in particular, to a self-dilating catheter introducer and obturator system for introducing implantable medical devices into a body cavity. Depending on the size of the orifice or opening in which the device is required to pass through determines the French scale size of the device (e.g. The French scale is a measure of the external diameter of a catheter not internal channel).

Abstract: A urine passing structure comprises a penis covering portion, a glans protection portion, and a urine guiding portion. The penis covering portion and the urine guiding portion are respectively fluidly communicated with the glans protection portion. A diameter of one end of the glans protection portion fluidly communicated with the penis covering portion is larger than the diameters of the penis covering portion and the urine guiding portion. It is tapered from a top end of the glans protection portion toward a tail end of the urine guiding portion. An accommodating space is defined in the glans protection portion. A passage is passing through the penis covering portion and fluidly communicated with the accommodating space. A urine guiding channel is passing through the urine guiding portion and fluidly communicated with the accommodating space. A one-way urine passing member is arranged in the urine guiding channel.

Abstract: A dental forceps that include an elongated handle and a pair of tooth engaging members or jaws extending out of the one end of the handle and a post located in the handle with a disc at the top with a ball at the other end of the post. The post ball end inserts into the post ball holder to provide a stable support so that the dentist has leverage to extract the tooth straight out. The post disc and post ball provide the forceps with side-to-side and back-and-forth movement, thus allowing the forceps to align to the growth angle of the tooth to be extracted.

Abstract: The application relates to needle protection assembly (1)) comprising:—a support (2) of the needle (3),—a needle shield (8) having a longitudinal axis A,—urging means (13) for displacing said needle shield (8) from a “in, use” position to a “after use” position,—a locking element (10) intended to prevent said needle shield (8) from moving back from its “after use” position to its “in use” position, characterized in that said locking element (10) has a longitudinal axis B and is radially movable with respect to said needle shield (8) between a “free” position, in which the longitudinal axis A of the needle shield (8) and the longitudinal axis B of the locking element (10) are merged and in which said needle shield (8) is movable from its “in use” position to its “after use” position, and a “locking position”, in which the longitudinal axis B is radially spaced apart from the longitudinal axis A and in which movement of the needle shield (8) from its “after use” position to its “in use” position is prevented.

Abstract: A needle that consists of two pieces: the first piece has a tip, a shaft, a spring and a bi-color indicator, and the second piece has two parallel hollow lumens; one lumen is for fluid entrance and passage, and the other lumen configured to receive the first piece. When the hypodermic needle tip touches the skin or being inside a tissue the spring will be squeezed and the first piece will be situated backward in its primary position. When the tip of the needle just enters any cavity or any vessel the spring will be freed and pushes the first piece forward with the change of the color of the bicolored indicator.

Abstract: A transseptal medical device is provided including a dilator, a needle, and a needle control mechanism. The needle may be disposed within the dilator, and the needle control mechanism may be operably connected to a proximal end of the needle or the dilator for selective adjustment of the distal end of the needle from a first position within the dilator to a second position external to the dilator. The needle control mechanism may include an actuator configured for rotation within the dilator in one embodiment. In another embodiment, the proximal end of the dilator may incorporate internal threads and the proximal end of the needle may incorporate external threads, such that the needle may be configured for rotation during selective adjustment of the distal end of the needle from a first position to a second position. A method for puncturing a septum of a heart is also disclosed.

Abstract: An infusion set has an adhesively secured main hub, and a slidable top cover, needle hub and angled or cantilevered needle that can be used for performing an intradermal needle insertion precisely targeting the upper 3 mm of skin surface, for example, one that substantially duplicates the Mantoux insertion technique, for injecting into the intradermal layers of skin, while maintaining a degree of comfort to the user. By sliding the top cover, the cantilevered needle is loaded and released or the angled needle is slid into an insertion site, while flexible arms and adhesive are used to stretch and/or flatten a skin surface, or otherwise create skin tension, at the insertion site.

Abstract: Apparatus, systems, and methods are provided for delivering a lead or other instrument into a patient's body using a tubular device including a proximal end, a distal end sized for introduction into a body lumen, and a lumen extending therebetween, thereby defining a longitudinal axis. The tubular device includes a sidewall surrounding the lumen including a reinforcing layer embedded in one or more layers of base material, and a slittable seam in the sidewall extending from the proximal end partially towards the distal end substantially parallel to the longitudinal axis. In addition, slitter devices are for slitting, splitting, or opening the slittable seam. Methods are also provided for making catheters or other tubular devices including slittable, e.g., re-welded longitudinal seams that may be preferentially slit, split, or otherwise opened.

Abstract: A wearable, self-contained drug infusion device is disclosed that is capable of achieving the precise flow rate control needed for dose-critical drugs such as insulin. In preferred embodiments of the device, at least two flow channels are utilized in conjunction with a series of valves for providing a user with selectable, constant flow rate control. The device can be made with small dimensions so that it can be worn by the user with a minimum of discomfort and inconvenience. In addition, the simple mechanical nature of the device provides the user with close control over the flow rate, which is required for safe and effective delivery of insulin and other drugs. Also, the absence of electronic components allows the device to be manufactured inexpensively. The device is provided with a first channel that is long and narrow, functioning as a flow restrictor. The first channel is preferably provided in a serpentine pattern.

Abstract: Apparatuses and methods for the prevention of bodily injuries through active monitoring of bodily postures, supporting a body while in or restricting a body from entering predetermined postures which heighten the body's susceptibility to injury, and alerting one or more entities (e.g., an apparatus user) of a body's susceptibility to injury is disclosed herein. In one embodiment, the method may include one or more operations including monitoring one or more bodily postures and/or bodily movements, storing data associated with bodily postures and/or bodily movements, determining a risk of injury associated with bodily postures and/or bodily movements, and alerting one or more entities when a risk of injury associated with bodily postures and/or bodily movements reaches a predetermined level.

Abstract: A needle system for penetrating to or passing thought an object or an organ comprising a semiconductor die, one or more needles, wherein the needles slide over the plane of the die, one or more actuators that move the needles relative to the die plane, and one or more actuator drivers controlled by a controller wherein the controller instruct the needle to penetrate into or to pass through and/or retract from the object or organ. The needle system is used for drug delivery or blood extraction or blood analysis or glucose measurements or blood measurements or nerve system stimulus treatment or hair removal or skin lesions removal.

Abstract: A stoma guard for ostomy patients that is applied directly to the ostomy pouch. The guard prevents blunt force trauma, helps the user conceal protruded stoma and protects against daily impacts that can harm stoma region. The stoma guard has no sharp corners to prevent leakage and to increase maneuverability. The stoma guard is comprised of a rigid semi circular dome shaped guard and a crescent shaped applicator that secures the guard directly to the ostomy pouch. The guard has a convex shape facing outward that protects the stoma area once secured to the ostomy pouch. The stoma guard is sized to conform around the upper part of the ostomy pouch where the stoma is located. The stoma guard includes an opening at the base permitting flow of waste material. The stoma guard does not need to be removed when emptying waste from the ostomy pouch.

Abstract: A shieldable needle device includes a hub with and a needle cannula having a puncture tip extending from a forward end thereof, and a shield member in telescoping association with the hub. At least one of the hub and the shield member are adapted for relative axial movement with respect to the other between a first position in which the puncture tip of the needle cannula is exposed from a forward end of the shield member and a second position in which the puncture tip of the needle cannula is encompassed within the shield member. A drive member extends between the hub and the shield member, biasing the hub and the shield member axially away from each other. A packaging cover may further extend about the needle cannula, applying external pressure between the cooperating portions of the hub and the shield.

Abstract: Methods and devices incorporating a guidewire entry port subassembly for use in rapid exchange catheters. The use of a subassembly allows for stronger quality control and simpler fabrication of a rapid exchange device. In several embodiments, methods of making a molded guidewire entry port using a mold, often in conjunction with one or more mandrels, are disclosed. Several device embodiments include a separate molded guidewire port as well as molded guidewire ports which are attached, during a molding step, to segments of a catheter.

Abstract: A soft dual-layer rectal speculum includes a main tube member having a distal end for insertion into a patient's rectum and a proximal end for connection to a waste removal hose where at least a portion of the main tube member includes an inner hard layer and an outer soft layer, and an inlet tube member for directing fluids into the main tube member. The inlet tube member may include a swivel mechanism and the portion of the main tube member having an inner hard layer and an outer soft layer may include a measurement gauge that is visible through the outer soft layer but can't be felt through the outer soft layer. A rectal speculum assembly includes the soft dual-layer rectal speculum described above and an obturator which includes an elongated member having a tapered distal end capable of extending through the distal end of the main tube member. The tapered distal end of the obturator may be made of a soft, pliable material or an inner hard layer (or member) and an outer soft layer.

Abstract: A connective tissue modification cuff can be applied around a portion of the body and drawn tight. Integrated within the portion of the cuff that is pressed against the body is a plurality of variable compression beads. These variable compression beads comprise half spherical beads, half prolate spheroid beads, half oblate spheroid beads, or other similarly rounded structures that provide variably increasing pressure towards their high-points and gradually reduced pressure towards their low points. The cuff can be tightened down via a tensioning system that allows even tightening in small increments. Once in place, the person then stretches or uses the arm in order to apply the variable compression beads to the connective tissue under use. Such application works on the underlying connective tissue to reduce the pain and associated problems.

Abstract: A microwave antenna assembly is disclosed. The antenna assembly includes a feedline having an inner conductor, an outer conductor and an inner insulator disposed therebetween. A radiating portion is also included having an unbalanced dipole antenna including a proximal portion and a distal portion that are of different lengths. The proximal portion includes at least a portion of the inner conductor and the inner insulator and the distal portion includes a conductive member.

Abstract: Disclosed herein is a high strength, bioresorbable wall thickness suitable for use in an endoprosthesis such as a stent that is produced by first forming a wall thickness by melt processing or solution processing one or more bioresorbable materials into a tubular shape; drawing the shape from shorter length to an optimum longer length and reducing the diameter from a larger diameter to a smaller diameter to orient the molecular chains of the material; fabricating a stent from the tube formed of the oriented material by cutting a strut pattern in its wall thickness; covering the stent's struts with at least one coating to delay degradation of the bioresorbable material; covering the stent's struts with one or more controlled release active ingredients to minimize the risk of restenosis or other side effects; crimping the stent onto a balloon catheter assembly; delivering the stent into an anatomical lumen via percutaneous methods to a treatment location; radially expanding the stent from a smaller size to a la

Abstract: An umbilical line-securing device adapted to nonadhesively maintain an umbilical line at a location relative to an umbilical stump.

Abstract: A battery management method for one or more batteries in a healthcare delivery system is provided. The method includes determining when the healthcare delivery system is drawing power from the one or more batteries and controlling a display unit coupled to the controller to display an initial number corresponding to a time remaining on battery (TROB) when the healthcare delivery system is drawing power from the one or more batteries. The method also includes determining if the TROB is within a reserve range extending up to a reserve range maximum that is less than a maximum TROB, changing the TROB according to an operational state of the healthcare delivery system if the TROB is greater than the reserve range maximum, and decreasing the TROB to count down the TROB without regard for the operational state of the healthcare delivery system if the TROB is less than the reserve range maximum.