194results about How to "Actuation can be prevented" patented technology

A surgical instrument particularly suited to endoscopic use articulates an end effector by including a laterally sliding member in a proximal portion of a shaft that pivots the end effector to a selected side. Differentially opposing actuating forces (e.g., hydraulic, fluidic, mechanical) act against the laterally sliding member without binding by incorporating guidance mechanisms between the laterally sliding member and a frame of the shaft.

There is provided a powered tacker device for use in installing multiple surgical fasteners through a prosthetic mesh into tissue. The powered tacker device generally includes a handle assembly and a tacker assembly extending distally from the handle assembly. The handle assembly includes a motor and self-contained power assembly to rotate the surgical fasteners into tissue. The handle assembly is provided with a drive assembly which allows for rotation, as well as distal longitudinal movement, of a surgical fastener relative to the powered tacker device. The tacker assembly includes an inner tube for containing the plurality of surgical fasteners and a driver which is movable out of alignment with the inner tube so as to install a single fastener at a time into tissue.

A circular stapler with an automatic safety mechanism comprises a stapler body, a stapler head, an actuating mechanism and a transmission adjusting mechanism; wherein the actuating mechanism comprises a handle and a handle coat, the transmission adjusting mechanism comprises a screw rod and an adjusting knob; a stopper is disposed either inside said handle or said handle coat; a safety rod and a pulling sheet are further provided, the safety rod has a safety block on one end and has a protruding block and a pin hole as its middle portion, a cylindrical pin is inserted into the pin hole so as to get the safety rod to be pivotally connected with the stapler body; the pulling sheet has a rear portion mounted on the screw rod and has a pulling hook at its front portion, the pulling hook hooks with the protruding block.

A surgical instrument particularly suited to endoscopic use articulates an end effector by including a laterally sliding member in a proximal portion of a shaft that pivots the end effector to a selected side. Differentially opposing actuating forces (e.g., hydraulic, fluidic, mechanical) act against the laterally sliding member without binding by incorporating guidance mechanisms between the laterally sliding member and a frame of the shaft.

An auto-injector for dispensing a predetermined dose of medicament is disclosed. The auto-injector includes a needle cover that is configured to move from a retracted position to an extended locked position. The auto-injector includes a first locking assembly to hold the needle cover in a locked retracted position and a second locking assembly to hold the needle cover in a locked extended position.

There is provided a powered tacker device for use in installing multiple surgical fasteners through a prosthetic mesh in into tissue. The powered tacker device generally includes a handle assembly and a tacker assembly extending distally from handle assembly. The handle assembly includes a motor and self-contained power assembly to rotate the surgical fasteners into tissue. The handle assembly is provided with a drive assembly which allows for rotation, as well as distal longitudinal movement, of a surgical fastener relative to the powered tacker device. The tacker assembly includes an inner tube for containing the plurality of surgical fasteners and a driver which is movable out of alignment with the inner tube so as to install a single fastener at a time into tissue.

A surgical clip applier is provided and includes a ratchet mechanism having a rack member connected to a drive channel such that axial translation of the drive channel results in axial translation of the rack member, the rack member defining a first set of teeth along a first side thereof and a second set of teeth along a second side thereof. The ratchet mechanism including a first pawl and a second pawl each tiltably supported in the housing and disposed on respective opposed sides of the rack member; and a buckling spring interposed between the first pawl and the second pawl and constrained in a slot formed in the rack member, wherein the buckling spring is dimensioned so as to bow in one of a proximal direction and a distal direction.

Methods, devices, and systems are provided for performing endovascular repair of atrioventricular and other cardiac valves in the heart. A delivery device for delivering an implantable device to a target area includes a fluid management system for directing fluid and delivery device components to the target area. The delivery device includes a grip line assembly configured to control a gripper in the implantable device for grasping tissue at the target area. The delivery device includes a lock line assembly configured to control a locking mechanism in the implantable device to lock the implantable device in a desired orientation. The delivery device includes a deployment handle configured to provide staged deployment of the implantable device. A delivery assembly includes a housing and a delivery device partially housed within the housing and being adjustable using one-handed operation.

A dispensing assembly is provided for a container of fluent material. A hand-operable dispenser cartridge is adapted to be mounted to the container. An actuator, which may include a nozzle or spout, is mounted on the cartridge. A locking sleeve is mounted around the cartridge and has an upper abutment edge and a recess. The locking sleeve can be rotated between a first rotated position preventing actuation of the dispensing assembly and a second rotated position permitting actuation of the dispensing assembly.

A locking-stressing-mechanism with spring-actuated output drive and a counter with which an apparatus of this kind is fitted, accommodated in a two part housing the two parts of which are mounted to be rotatable relative to each other, can be blocked by means of a pre-stressed leaf spring. The leaf spring is initially accommodated in a recess in the wall of one housing part. As soon as the permitted number of actuations has been reached a push rod pushes the leaf spring out of its resting position. The leaf spring then jumps into a recess in the wall of the other housing part and the two housing parts can no longer be rotated relative to each other. The push rod may be mounted on the pointer of the counter. This blocking device can only be overcome by the application of a force which is sufficient to destroy the device. The device is suitable for blocking a high pressure atomiser or a needleless injector with which a fluid is atomised to form an aerosol or a fluid is injected into a biological tissue.

A device for removing fluid from a first bodily cavity and for directing that fluid into a second bodily cavity while avoiding risks of infection and, in one embodiment, excessive dehydration of the first bodily cavity. The device includes an uptake tube having a proximal end in fluid communication with the first bodily cavity and a distal end in fluid communication with a pump, and an outflow tube having a proximal end in fluid communication with the pump and a distal end in fluid communication with the second bodily cavity. The distal end of the uptake tube may be coupled to a reservoir configured to expand upon ingression of fluid into the reservoir and to contract upon removal of fluid due to a negative pressure provided by the pump.

A dispensing assembly is provided for a container of fluent material. A hand-operable dispenser cartridge is adapted to be mounted to the container. An actuator, which may include a nozzle or spout, is mounted on the cartridge. A locking sleeve is mounted around the cartridge and has an upper abutment edge and a recess. The locking sleeve can be rotated between a first rotated position preventing actuation of the dispensing assembly and a second rotated position permitting actuation of the dispensing assembly.

The invention concerns a system wherein the tool-bearing frame (1) and the tool (2) are each equipped with a multiple fluidic connection box, for example hydraulic provided with complementary male-female connecting members: each of said boxes is provided with a mobile and retractable protective cover, which normally covers the connecting members contained in said box. Said covers are arranged such that, in a first phase, the proper positioning of the tool-bearing-frame opposite the tool automatically causes the covers to retract, directly matching the fluidic connection members of the two boxes, so as to enable subsequently, in the second and third phases, the mechanical followed by the fluidic connection of the tool-bearing frame and the tool. The system protects the connecting members from the outside environment, while enabling easy and secure connection of the tool with the tool-bearing frame, without any risk of deterioration of the fluidic connectors.

Methods, devices, and systems are provided for performing endovascular repair of atrioventricular and other cardiac valves in the heart. A delivery device for delivering an implantable device to a target area includes a fluid management system for directing fluid and delivery device components to the target area. The delivery device includes a grip line assembly configured to control a gripper in the implantable device for grasping tissue at the target area. The delivery device includes a lock line assembly configured to control a locking mechanism in the implantable device to lock the implantable device in a desired orientation. The delivery device includes a deployment handle configured to provide staged deployment of the implantable device. A delivery assembly includes a housing and a delivery device partially housed within the housing and being adjustable using one-handed operation.

An auto-injector for dispensing a predetermined dose of medicament is disclosed. The auto-injector includes a needle cover operative to engage an injection site. The needle cover is configured to move from a retracted position prior to a medicament dispensing operation to an extended locked position after the medicament dispensing operation. Any residual activation force remaining after the medicament dispensing operation is contained within the auto-injector and is not directed to the needle cover, thus attenuating, if not eliminating, any kickback effect.

Devices, methods and systems are provided for occluding an opening within the tissue of a body, such as a left atrial appendage. In one embodiment, a system for use in occluding an opening in the tissue of a body includes a handle, a catheter coupled with the handle and a medical device disposed within a lumen of the catheter. The medical device includes an anchor system having a plurality of anchor segments coupled with an anchor hub. The medical device further includes an occluder system having a plurality of occluder segments coupled with an occluder hub. A first actuator is configured to displace the occluder hub independent of, and relative to, the anchor hub to deploy the occluder system from a refracted state to an expanded state while the anchor system remains in a retracted state.

An auto-injector automatically dispenses a predetermined dose of medicament upon activation. The auto-injector includes a needle cover operative to engage an injection site and activate the injector. The needle cover is configured to move from a locked retracted position prior to a medicament dispensing operation to a locked extended position after the medicament dispensing operation. The non-removable needle cover prevents contact with the needle both before and after the medicament dispensing operation.

A surgical stapling device is disclosed for performing circular anastomoses. The surgical stapling device includes a handle portion, an elongated body portion and a head portion including an anvil assembly and a shell assembly. The head portion includes an anvil assembly including a tiltable anvil which will tilt automatically after the device has been fired and unapproximated. The tiltable anvil provides a reduced anvil profile to reduce trauma during removal of the device after the anastomoses procedure has been performed. The stapling device includes an approximation mechanism including a rotatable knob, a screw having a helical channel and an anvil retainer. The helical channel includes a dwell portion for providing a tactile indication to a surgeon that the anvil retainer has been advanced to a position wherein the anvil assembly can be removed from the anvil retainer. A removable trocar for attachment to the anvil assembly is also disclosed which includes a rib positioned proximally of a mounting projection. The rib is positioned to align the mounting projection with associated engagement structure of the anvil assembly.

A device for removing fluid from a first bodily cavity and for directing that fluid into a second bodily cavity while avoiding risks of infection and, in one embodiment, excessive dehydration of the first bodily cavity. The device includes an uptake tube having a proximal end in fluid communication with the first bodily cavity and a distal end in fluid communication with a pump, and an outflow tube having a proximal end in fluid communication with the pump and a distal end in fluid communication with the second bodily cavity. The distal end of the uptake tube may be coupled to a reservoir configured to expand upon ingression of fluid into the reservoir and to contract upon removal of fluid due to a negative pressure provided by the pump.

Abstract of Disclosure A control system for a paintball marker having a breech, the control system comprising a contact sensor, a controller, and a paintball firing mechanism, the sensor being arranged to be located within the paintball marker, to sense a paintball being in contact therewith, and to produce a signal indicative of the presence of said paintball within said breech, and the controller being arranged to receive said signal and to control the actuation of said firing mechanism in response to said signal.

A vehicular safety apparatus of the present invention is one actuated according to a collision prediction level of a vehicle. The vehicular safety apparatus of the present invention is provided with a determining device for determining a collision prediction level on the basis of a relative position between a vehicle and an obstacle ahead of the vehicle; a storage for storing a amount of brake operation by a driver at a point where the collision prediction level exceeds a predetermined threshold, as a reference level; and an actuation controller for actuating the safety apparatus in accordance with an increase from the reference level. This prevents the actuation of the safety apparatus from being excessive in the case where an increase of the amount of brake operation is low. Furthermore, in the case of the increase being high, the actuation is controlled so as to fully bring out the performance of the safety apparatus. Therefore, the performance of the safety apparatus can be suitably demonstrated without causing the driver to feel odd.

An ECU executes a program including: steps of detecting an SOC and a temperature TB of a traction battery; when an EV switch is on, a step of calculating a temperature correction coefficient α from TB; when EV switch not on, a step of calculating a temperature correction coefficient α from TB; steps of calculating an EV traveling allowed power value WOUT based on the SOC and the temperature correction coefficients; and a step of transmitting EV traveling allowed power value WOUT to a meter ECU in order to indicate EV traveling allowed power value WOUT on a power meter.

A membrane switch provides a substantially rigid front fascia without the need for flexure limiting standoffs or the like. The membrane switch may use thin, printed insulating dots whose pattern controls the force required to actuate the switch elements as a function of distance from the switch elements preventing multiple activations.

A surgical instrument may have a handle, a support sleeve, and an inner sleeve. Illustratively, the support sleeve may be configured to actuate relative to the inner sleeve to protect the inner sleeve before and after a surgical procedure and to expose a portion of the inner sleeve during the surgical procedure. In one or more embodiments, an application of a force to a distal end of the support sleeve may be configured to retract the support sleeve relative to the inner sleeve. Illustratively, a reduction of a force applied to the distal end of the support sleeve may be configured to extend the support sleeve relative to the inner sleeve.

A system for preventing inadvertent actuation of a medical device. The system includes an elongate tube having a proximal end, a distal end, and a lumen extending from the proximal end to the distal end. The lumen is configured to receive a medical device configured to transition between an actuated state and an inactive state. The device further includes a detection system configured to determine a position of a distal end of the medical device relative to the distal end of the elongate tube. The detection system includes a transmitting element and a receiving element.

A relay is designed to be used in a circuit where the voltage levels are high in comparison to the spacing between the contacts when open. Contact closure arcing is suppressed by actuating a MOSFET that shorts the contacts together while they open. The same MOSFET can momentarily short the contacts together just before they first begin to close, allowing a test current to be passed through the MOSFET and through the terminals connecting to both relay contacts, to insure that arc suppression will be successful; and if this test fails, then the relay can be disabled by a switch in series with the relay coil to prevent arcing and a possible fire hazard. Relay deactuation can be sensed to trigger arc suppression, and relay actuation can be sensed to initiate fail-safe testing by a circuit that responds no matter which way the relay coil is connected into the external circuit that drives it.

A child-resistant closure system for a container includes an overcap having a pair of levers, each opposite the other and formed into a side facing of the overcap, each lever including a lower vertical member on a rear side thereof, the overcap including a pair of partial threads extending horizontally along an inner surface at the bottom of the overcap, each partial thread 180 degrees from the other, and a cylindrical collar configured to receive the overcap thereon, the collar having an opening configured to receive a dispenser tip and bottleneck of the container therethrough, the collar forming a mechanical bond with the bottleneck, the collar including a neck having a pair of neck threads formed around an external surface thereof, each neck thread 180 degrees apart from the other on the neck, each neck thread terminating at a truncated vertical wall formed on the neck external surface.