A61B50/20

Devices for supporting a medical instrument and methods of use
11547517 · 2023-01-10 ·

Various implementations include a device for holding and supporting a medical instrument in a position. For example, the medical instrument may include a percutaneous procedure apparatus, such as a needle (e.g., biopsy needle, anesthesia needle) or needle holder. In some implementations, the device holds and supports the percutaneous procedure apparatus and liberates the procedure operator's hands from direct beam exposure, which lowers the risk of complications and radiation exposure to patients and procedure operators. The device also increases the effectiveness of the procedure by holding and supporting the apparatus in the intended position.

Devices for supporting a medical instrument and methods of use
11547517 · 2023-01-10 ·

Various implementations include a device for holding and supporting a medical instrument in a position. For example, the medical instrument may include a percutaneous procedure apparatus, such as a needle (e.g., biopsy needle, anesthesia needle) or needle holder. In some implementations, the device holds and supports the percutaneous procedure apparatus and liberates the procedure operator's hands from direct beam exposure, which lowers the risk of complications and radiation exposure to patients and procedure operators. The device also increases the effectiveness of the procedure by holding and supporting the apparatus in the intended position.

Packaged medical device
11547518 · 2023-01-10 · ·

To provide a packaged medical device in which a medical device in a container is stably fixed and which can be easily opened. Specifically, provided is a packaged medical device comprising a container having an opening portion and a flange portion formed to extend outward in a peripheral portion of the opening portion, a medical device housed inside the container, and a lid member having a gas impermeable film and peelably heat-sealed to the flange portion, in which the inside of the container is set to a negative pressure to the atmospheric pressure so that the medical device is pressed by the lid member and the peel strength to the flange portion of the lid member is 2 to 50 N/in.

Trackable protective packaging for tools and methods for calibrating tool installation using the same

Protective packaging, surgical kits, systems, and methods are described herein for assisting in determining whether a tool is properly installed on a surgical device. The protective packaging retains the tool and has trackable features defined relative to a tool center point of the tool. The trackable features have a predetermined state defined relative to the tool center point and the trackable features are configured to be detectable by a localizer to locate the tool center point. One or more controllers can compare the actual state of the tool center point with an expected state of the tool center point, which is based on an expected condition in which the tool is properly mounted to the surgical device. Based on the comparison, the one or more controllers can determine whether the tool is properly mounted to the surgical device.

Packaged medical device and method for manufacturing packaged medical device
11540892 · 2023-01-03 · ·

To provide a packaged medical device which is hard to cause a variation in the fixed states of the medical devices. Specifically, provided is a packaged medical device comprising a container having an opening portion, a medical device housed inside the container, and a gas impermeable film sealing the opening portion by heat-sealing, in which the inside of the container is set to a negative pressure to the atmospheric pressure and the medical device is pressed by the gas impermeable film.

Surgical access system including instrument retaining clip

A surgical access system includes a clip, a cannula, and an obturator. The clip includes a first housing half and a second housing half. The first and second housing halves have first end portions pivotably coupled together and second end portions having respective first and second fastener portions. The clip is movable between an open position in which the second end portions are spaced apart from each other and a closed position in which the first and second fastener portions of the second end portions are engaged with each other. The cannula and the obturator are retained between the first and second housing halves when the clip is in the closed position.

System for preparing a harvested blood vessel for grafting
11540816 · 2023-01-03 ·

A system for preparing a harvested blood vessel for use as a graft during a coronary artery bypass procedure, which includes an elongated platform, a mounting flange extending upwardly from a top surface of the platform adjacent a proximal end thereof for supporting a syringe in a fixed position, and a pair of longitudinally spaced apart clamp holders operatively associated with the top surface of the platform, each clamp holder configured to support a respective vessel clamp, wherein the vessel clamps supported within the clamp holders are adapted to hold a harvested blood vessel immobile therebetween so it can be prepared for grafting.

ASSEMBLY COMPRISING A MEDICAL DEVICE ADAPTED TO BE IMPLANTED AND PACKAGING FOR SAID DEVICE

The invention relates to an assembly formed by a medical device (1) adapted to be implanted in a human or animal body and by packaging, wherein: te medical device comprises a housing (11) that encloses a fluid reservoir (13) and a fluid outlet (12) forming a fluid connection between the reservoir and a volume outside the housing; the packaging includes a tank (2) comprising a bottom (20), a side wall (21), an upper face opposite the bottom in a vertical direction, and an opening configured to fill the tank with a biocompatible fluid, the bottom (20) of the tank extending in a horizontal plane perpendicularly to the vertical direction; at least one of the bottom, the side wall and the top face comprises a first holding element (201) adapted to hold the housing in the tank, the housing (11) being held in the tank (2) by said first holding element (201) such that the reservoir is located between the bottom of the tank and the fluid outlet, said fluid outlet being arranged below the opening such that the fluid outlet is immersed in the fluid when the tank is filled with the biocompatible fluid.

OMMAYA RESERVOIR TRAY FOR INSTALLATION OF INTRAVENTRICULAR CHEMOTHERAPY AND/OR ASPIRATION OF CEREBROSPINAL FLUID FOR DIAGNOSTIC PURPOSES
20220409322 · 2022-12-29 ·

A number of variations may include a sterile kit that may include a tray constructed and arranged to hold the necessary items to access an Ommaya reservoir and the tray may define a plurality of other resources or indentations constructed and arranged to seat, hold, or house additional components of the sterile kit. The sterile kit may additionally include a paper towel, a fenestrated drape, a plurality of sponge applicators, at least one pouch of povidone-iodine, at least one retractable winged butterfly needle, at least one luer lock syringe, a 3-way stopcock, a plurality of collection vials with tops which may be screwed on to prevent the contents thereof from leaking or escaping, sterile pads, bandages including adhesive bandages, and other components.

ASSEMBLY COMPRISING A TRANSER TOOL, AND TRANSFER TOOL
20220401172 · 2022-12-22 ·

The invention relates to an assembly comprising a sampling device with a rod and a swab and a transfer tool for detaching the swab from the rod and transferring the detached swab to a container. The transfer tool comprises a housing enclosing a closed chamber having a swab-member passage and configured for receiving the swab-member. The housing comprises a first housing part and second housing part hinged to the first housing part. The first housing part and second housing part define an entry opening to a channel delimited by the first and second housing part. This channel extends from outside the housing to the passage. The first housing part and second housing part are rotatable around the hinge between a holding condition and a non-holding condition. The swab-member passage is configured to prevent, in holding and non-holding condition, the base from entering the passage whilst allowing, in non-holding condition, the swab member to pass through the passage. The channel and swab are configured to allow, in non-holding condition, inserting the swab-member and the base through the entry opening into the channel, advancing the swab-member to and through the passage into the chamber until the passage prevents the base from entering the passage, and to prevent, in holding condition whilst the passage blocks the base in the insertion direction and the swab-member projects through the passage into the chamber, the base from movement opposite to the insertion direction.