1192results about How to "Prevent insertion" patented technology

An electromechanical surgical device is provided and includes an end effector configured to perform at least one function; and a shaft assembly. The end effector includes a rotatable drive screw having a coupling member at a proximal end thereof; and a flexible drive cable rotatably supported therein and extending therefrom, wherein the flexible drive cable receives rotational forces and transmits said rotational forces to the drive screw to actuate the end effector. The shaft assembly includes a proximal neck housing supported at a distal end of the outer tube; and a distal neck housing pivotally connected to the proximal neck housing, wherein a distal end of the distal neck housing is configured and adapted for operative connection with the end effector. In use, when the end effector is connected to the shaft assembly, the flexible drive cable extends through the proximal neck housing and the distal neck housing.

An electromechanical surgical device is provided and includes an end effector configured to perform at least one function; and a shaft assembly. The end effector includes a rotatable drive screw having a coupling member at a proximal end thereof; and a flexible drive cable rotatably supported therein and extending therefrom, wherein the flexible drive cable receives rotational forces and transmits said rotational forces to the drive screw to actuate the end effector. The shaft assembly includes a proximal neck housing supported at a distal end of the outer tube; and a distal neck housing pivotally connected to the proximal neck housing, wherein a distal end of the distal neck housing is configured and adapted for operative connection with the end effector. In use, when the end effector is connected to the shaft assembly, the flexible drive cable extends through the proximal neck housing and the distal neck housing.

A surgical stent made of biocompatible material for implantation in human tissue to enable blood and nutrients to flow from an area of vascular tissue to an area of tissue with little or no vasculature.

A personal identification device and method prevent the reduction in the finger vein recognition rate which otherwise occur due to erroneous insertion of a finger by a user not accustomed to operation or insertion of a false finger at low cost. The device includes an imager picking up an image of a finger vein pattern, a light source emitting light adapted to be transmitted through the finger, an image operating unit matches the image, guides indicating the position of picking up the finger image, a detector detecting the contact between the finger and the guides, another light source radiating light reflected from the thick of the finger, a switch which is depressed by the forward end of the finger, a further light source emitting light transmitted through the forward end of the finger, and a light-sensor receiving the light from the further light source through the finger.

A surgical fastener applying apparatus for applying fasteners to body tissue. The apparatus includes a cartridge receiving half-section defining an elongated channel member configured to releasably receive a stationary housing of a firing assembly. The stationary housing is dimensioned to releasably receive a single use loading unit therein, and includes a lockout structure that prevents insertion of the single use loading unit into the stationary housing after the stationary housing is mounted to the cartridge receiving half-section.

The present invention generally provides improved medical devices, systems, and methods. Embodiments may be particularly well suited for the treatment of dermatological and / or cosmetic defects, and alternative embodiments may be configured for treatment of a wide range of target tissues. Some embodiments of the present invention apply cooling with at least one small, tissue-penetrating probe, the probe often comprising a needle having a size suitable for inserting through an exposed surface of the skin of a patient without leaving a visible scar. The cooling may remodel one or more target tissue so as to effect a desired change in a composition of the target tissue and / or a change in its behavior. Exemplary embodiments make use of replaceable needle probes supported by a probe body handle, with small needle probes often being replaced during treatment of a single patient. Unlike the large format cryogenic cooling systems of the past, small cryogenic cooling needle probes may dull or be damaged by insertion. Careful control over the control of cryogenic cooling fluid into a needle probe can allow the length of the active cooling to be controlled through depletion of liquid from an evaporating cryogenic cooling flow. Hence, even needles having similar external structures may provide differing lengths of an iceball along the needle axis. Surprisingly, small cryogenic cooling needles and / or other cryogenic cooling probes having a lubricious coating will allow safe removal of the probe from the treatment region while at a least a portion of the tissue remains frozen, significantly decreasing the overall time for a procedure involving many insertion / freeze / removal cycles.

The present invention is directed to a data cartridge library system that realizes a reduced cost by reducing the number of certain components, especially expensive components, that are needed to perform certain functions within the library. With respect to certain functions, a reduced cost is realized by using lower precision componentry in combination with componentry that compensates for lower precision while still providing a reduced component cost with respect to a given function. In one embodiment of the invention, a data cartridge picker is provided that: (1) uses a single electro-mechanical device for the functions of grasping a data cartridge, retracting a grasped cartridge from a drive / storage location, inserting a grasped cartridge into a drive / storage location, and releasing a grasped cartridge once position in a desired location; (2) is capable of compensating for variations in cartridge positioning; (3) has a gripping mechanism that moves in a sinusiodal manner; and (4) avoids the wear and tear associated with moving fully retracted gripper mechanism that is not holding a data cartridge from a fully retracted position to a position at which a cartridge can be retrieved. Another embodiment provides a elevator mechanism for moving the cartridge picker in which the guiding portion of the mechanism is also part of the portion of the mechanism that moves the cartridge picker. A further embodiment employs a face plate extension that facilitates insertion of a data cartridge into a drive by a low precision cartridge transport device. Yet another embodiment provides a removable data cartridge holder that: (1) includes a box-like structure for holding data cartridges and a dust cover that can be placed over the opening of the box-like structure when the holder is not in use and when the holder is in use, attached to the box-like portion; (2) an orientation structure that prevents insertion of a data cartridge into the box-like holder if the cartridge is improperly oriented; and (3) retention clips for preventing accidental dislodgement of a data cartridge located in the box-like structure.

The present disclosure relates to a surgical fastener applying apparatus for applying fasteners to body tissue. The apparatus includes a cartridge receiving half-section defining an elongated channel member configured to releasably receive a firing assembly and a single use loading unit. A lockout structure prevents insertion of the single use loading unit into the channel member after the firing assembly is mounted to the cartridge receiving half-section. Alternatively, the lockout structure prevents full insertion of the firing assembly into the cartridge receiving half-section, if the single use loading unit is not engaged with the firing assembly.

An improved drink can is disclosed wherein the drink can has a drink opening and a vent opening which are positioned opposite from each other with respect to a central portion of a top end of a drink can. The tab is attached to the central portion and can be pulled upward to open the drink opening then pushed back downward to open the vent opening. To aid in opening the vent opening with the tab, the vent opening may have a ridge to provide additional leverage when the tab pushes downward on a score line that defines the vent opening. The tab may be enlarged so that upon breakage of the score line to the vent opening, the tab contacts the top end of the can and does not allow the user's finger to proceed into the vent opening and possibly cut the user's finger.

A surgical drill assembly is provided that includes an elongate shaft having a proximal end adapted to mate to a driver mechanism, and a distal end having a bone preparation element formed thereon. An elongate, hollow sleeve is coupled to, but slidably disposed around at least a portion of the elongate shaft. The hollow sleeve includes a stepped region that is positioned between proximal and distal portions such that the distal portion has an outer diameter that is less than an outer diameter of the stepped region to allow the distal portion to be disposed within a lumen in a drill guide, and the stepped region to abut the drill guide. In use, the elongate, hollow sleeve is effective to longitudinally align the elongate shaft therein during a surgical procedure. The elongate shaft can also optionally include a stop member that is effective to limit penetration depth of the bone preparation element with respect to the hollow sleeve.

A device for cleaning the ear canal of cerumen or contaminants includes a handle, a material expandable upon exposure to a fluid, and a limiter connected to the handle operative to prevent insertion of the expandable material into the ear to a depth which could contact the ear drum. Fluid is passed through the handle and through apertures to the ear canal, and or to the expandable material, whereby the ear canal and expandable material are moistened. The expandable material expands to contact the ear canal walls and cerumen, whereby the cerumen may be extracted by withdrawing the handle and connected expandable material from the ear. The fluid may be an alcohol solution, which loosens cerumen, reduces the potential for infection, and promotes drying of the ear canal.

This present invention generally relates to devices and methods for repairing an aperture in a biological tissue. In certain embodiments, the invention provides a system for closing an aperture in a biological tissue including a handle, an elongate shaft connected to the handle, and a deployment scaffold connected to the shaft, in which the scaffold is configured to releasably retain a surgical implant and the scaffold is configured to deploy and attach the surgical implant to the biological tissue.

An integrated grip and rail system is provided. Included is a firearm and the firearm grip. The grip is configured to be disposed in front of the magazine well and provide a stable grip point which does not allow a user's thumb or other appendage to be disposed between the grip and magazine well. The grip is configured so as to not interfere with the pivoting relationship between the weapon upper and weapon lower during partial or complete disassembly of the weapon. The rear region may also have a portion extending rearward along at least part of each side of the magazine well to form feed ramps as a part of the magazine well extension. Included is a magazine well extension mechanically coupled to a forearm rail system for mounting to the firearm.

A tamper resistant assembly provides tamper resistance to an electrical receptacle. The tamper resistant assembly includes a base member having first and second grooves. Each groove has a first portion and a second portion connected to the first portion. The first portion is substantially perpendicular to a rear wall of the member and the second portion forms an angle with the first portion. A shutter member is slidably and pivotally connected to the base member for movement between open and closed positions. First and second protrusions extend outwardly from the shutter member and are slidably and pivotally received in the first and second grooves, respectively, in the base member. The first and second protrusions are disposed in the first portions of the grooves when the shutter member is in the closed position and prevent lateral sliding movement of the shutter member to prevent insertion of a foreign object past the shutter member, and in the second portions when the shutter member is in the open position by allowing lateral sliding of the shutter member. The first portions prevent lateral movement of the shutter member and allow pivoting movement of the shutter member to positions preventing insertion of a foreign object past the shutter member.

This present invention generally relates to devices and methods for repairing an aperture in a biological tissue. In certain embodiments, the invention provides a system for closing an aperture in a biological tissue including a handle, an elongate shaft connected to the handle, and a deployment scaffold connected to the shaft, in which the scaffold is configured to releasably retain a surgical implant and the scaffold is configured to deploy and attach the surgical implant to the biological tissue.

A fluid connection assembly (10) includes a metal tube (22) having a flared end and a plastic manifold (12) having a port (14). The port (14) includes an annular collar (16) and an annular recess (18) that receives a seal (20). The metal tube (22) is arranged over the port (14) and engages the seal (20). The flared end of the metal tube (22) abuts the annular collar (16) of the port (14) when the metal tube (22) is installed. A plastic retainer (28) is molded over the annular collar (16) of the port (14) and the flared end of the metal tube (22) to retain the metal tube (22) axially on the port (14) of the manifold (12). Alternately, the end (221) of the metal tube (222) is crimped to secure the metal tube (222) to the port (214) of the manifold (212).

A user-mode device driver architecture is provided by the subject invention. The architecture includes a reflector, a driver manager and a host process which hosts and isolates one or more user-mode device driver(s). The user-mode device driver runs in the user-mode (UM) environment and has access to various UM services. The reflector resides in “kernel memory” (e.g., memory / resource(s) available to operating system) while the driver manager, host process and user mode device driver(s) are located in user space (e.g., memory / resource(s) available to user application(s)). The reflector provides a secure, stable communication path for application(s), the host process and / or user-mode device driver(s) to communicate with the operating system. The reflector can redirect input / output (I / O) request(s) from application(s) to the user-mode device driver(s) via the host process. The driver manager can create the host process (e.g., in response to a request from the reflector), track information about the host process and / or destroy the host process (e.g., in response to a request from the reflector).

The invention provides a real-time three-dimensional reconstruction key frame determination method based on position and orientation changes. The method is achieved through four steps of current frame positioning, positioning quality evaluation, view difference calculation and judgment on whether key frames are inserted or not. The method has the advantages that the key frames are high in quality, speed and stability, and the insertion of a wrong frame can be effectively prevented by judging the positioning quality of image frames; meanwhile, the view difference concept is put forward, it is ensured that each inserted key frame includes certain new image information through the corresponding view difference threshold values, redundancy between the key frames is effectively reduced, and burdens on map establishment are reduced.

An electrical connector includes an insulative housing (1), a plurality of contacts (2), and a shell (3) surrounding the housing. The insulative housing includes a base portion (10) with a plurality of passageways (111) extending therethrough, a tongue portion (12) extending forwardly from the base portion, and a rib (11) formed at an end of the tongue portion. A plurality of terminals are received in the passageways and extend forwardly for dividing the tongue portion into several parts. Each terminal comprises a conductive surface (22, 23). The rib extends adjacent to one of the terminals and partially protrudes beyond the conductive surface of the one of the terminals.

An ESD protection device including a transistor structure with resistive regions located within active areas thereof. The transistor structure is formed of one or more MOS transistors, preferably N-type MOS transistors. The drain regions of the transistors are modified to reduce the conductivity of those resistive regions by preventing high carrier concentration implants in one or more sections of the drain regions. This is achieved by modifying an N LDD mask and the steps related thereto, as well as a silicide exclusion mask and the steps related thereto. The modifications result in the omission of N LDD dopant from the area immediately adjacent to the underlying channel. In addition, portions of a spacer oxide remain over the drain region to be formed. Subsequent implant and siliciding steps are effectively blocked by the spacer oxide that remains, leaving a low-density drain (LDD) charge carrier concentration in those regions, except where omitted. The resistivity of those resistive LDD regions is greater than the resistivity of the adjacent portions of the drain region. The result is more uniform turn-on of ESD transistor fingers in a protection device set without the need to add valuable layout space and without increased processing steps.

A button head tie has a button head and a tie strap. The button head is a generally flat member having an aperture for receiving the tie strap. The aperture includes lead-in ramps to facilitate tie strap insertion and is configured to prevent angled tie strap insertion. The tie strap is a flat elongate member having a wedge that is captured within the aperture. The remainder of the strap passes through the aperture. The wedge and strap have teeth and serrations on both sides, respectively, the teeth and serrations being engageable. In use, the strap is looped around a bundle and inserted into the aperture to either side of the wedge. Strap insertion force is reduced by standoff tabs which elevate the wedge out of aperture, temporarily, during installation. When loop tension is applied to the bundle, the wedge is pulled into the aperture, compressively locking the strap.

An emergency multi-medication pump injection system is designed for use in rapidly and automatically calculating and administering multiple medications in an emergency setting. The system includes a compact, portable housing comprising a plurality of medication ports, each port configured to receive a corresponding ampoule containing a corresponding medication. The system further includes at least one pump on or within the housing for dispensing a calculated dosage amount of one or more medications from the ampoules, at least one delivery tube for conveying the medication(s) from the system for delivery to the patient, and safety means for ensuring that each ampoule can only be installed in a port to which the particular ampoule corresponds. The pump injection system may include data inputs for inputting data relating to patient weight, medication concentration, medication dosage, and the like.

Disclosed herein are wearable devices for dispensing insect repellents, fragrances, and / or other chemicals along the outside of the clothing of a human, to avoid the need to apply such chemicals directly to clothing or to human's skin. The devices have an on / off switch that automatically controls a shutter which enables and restricts air flow, while also controlling fan operation and covering of a use-up cue. The device also is designed to prevent fan operation when an impregnated slab is not present. Also disclosed are preferred refills for use with such devices.

One or more external magnets that are suitable for placement on the back or front of a patient's neck and methods for using the external magnet(s) to guide a feeding tube containing one or more internal magnets through the esophagus are described herein. The external magnet is applied to the back or the front of the patient's neck and the feeding tube is inserted into the patient's nose and advanced within the patient's body. The magnetic field of the external magnet combines with the magnetic field of the internal magnet to produce a sufficient magnetic force to pull or push the feeding tube apparatus against the posterior wall of the esophagus to prevent placement of the stylet in the patient's trachea or windpipe to prevent insertion into the patient's lungs.