B29L2031/7546

Devices for Vascular Occlusion

An occlusive device, occlusive device delivery system, method of using, and method of delivering an occlusive device, and method of making an occlusive device to treat various intravascular conditions is described.

REUSABLE ULTRASONIC TRANSDUCER AND GENERATOR ASSEMBLIES, SURGICAL INSTRUMENTS INCLUDING THE SAME, AND METHODS OF MANUFACTURING THE SAME

An ultrasonic transducer and generator (TAG) assembly of a surgical instrument includes generator components and transducer components. The generator components are disposed within a first cavity cooperatively defined by a body portion and a cover. The generator components are covered in a thermally insulative material. The transducer components are disposed within a second cavity cooperatively defined by a proximal housing and a spinner housing.

Surgical stapler buttress assembly with adhesion to wet end effector

A buttress assembly is configured to temporarily adhere to a wet surgical stapler end effector. The buttress assembly includes a buttress body and a humidity tolerant adhesive material. The humidity tolerant adhesive material is applied to at least one side of the buttress body. The humidity tolerant adhesive material is configured to hold the buttress body to an underside of an anvil or a deck of a staple cartridge for at least five minutes in an environment of 100% relative humidity at approximately 37° C.

Fiber reinforced composite stents

Polymeric composite stents reinforced with fibers for implantation into a bodily lumen are disclosed.

Method of manufacturing a surgical instrument or prosthesis

A method of manufacturing a surgical instrument or prosthesis and an injection moulded surgical instrument or prosthesis are described. A first material is injected into a first mould to form an interim component. A second material is injected into a second mould containing at least part of the interim component to form the surgical instrument or prosthesis such that portions of the first and second materials are exposed at the external surface of the surgical instrument or prosthesis. The first and second materials are visually distinct such that at least one exposed portion of the first or second material adjacent to an exposed portion of the other material forms a marking which is visible to a user.

Electronic skin, preparation method and use thereof

The invention provides a piezoresistive electronic skin, a preparation method and a use thereof. The piezoresistive electronic skin uses carbon nanotube film as the conductive layer and uses materials provided with micro-nano patterns, such as polydimethylsiloxane, polyethylene terephthalate, polyvinyl alcohol, polyvinyl formal, polyethylene, and so on, as the substrate, enabling the substrate has advantages of high flexibility and being pliable, and it needs low operating voltage and little power consumption, but has high sensitivity and short response time. More importantly, the invention uses the patterned flexible substrate as the basis, greatly improving the sensitivity of electronic skin reacting to tiny applied force from outside. The invention also provides a capacitive electronic skin and a preparation method thereof. Further, the invention also provides a use of the piezoresistive electronic skin or the capacitive electronic skin on speech recognition, pulse detection, medical robot, etc.

Resurrection Of Antibiotics That MRSA Resists By Silver-Doped Bioactive Glass-Ceramic Particles

A bioactive scaffold is provided. The bioactive scaffold includes an interconnected web of struts composed of a glass-ceramic material, the web of struts being printed as a three-dimensional structure from a filament composition having a bimodal distribution of glass-ceramic microparticles, wherein the bioactive scaffold has a porosity defined by spaces between struts of greater than or equal to about 40% to less than or equal to about 80% and an average pore size of greater than or equal to about 200 μm to less than or equal to about 400 μm. Methods of making the bioactive scaffold and treating bone defects using the bioactive scaffolds are also provided.

METHOD OF DETERMINING LAYER THICKNESSES OF 3D MODELS FOR ADDITIVE MANUFACTURING
20220207829 · 2022-06-30 · ·

The present invention relates to a method of determining layer thicknesses (t) of a three-dimensional model (1) for generation with an additive manufacturing apparatus, the method comprising: a step of determining the layer thicknesses (t) according to an adaptive slicing algorithm in which the thickness of a layer (2) is calculated through a relation based on the inclination of the normal vectors (n) of the surface elements (s) of the 3D model (1) which at least partly enclose the layer (2) from a horizontal direction (x; y) the method being characterized by further comprising: a step of selectively imposing on at least one surface element (s) of the 3D model (1) a precision requirement out of one or more selectable different precision requirements which respectively differently alter in the determination step the relation with respect to the inclination of the normal vector (n) of the said at least one surface element (s) which allows, through the altered relation, the layer thickness (t) to obtain a value smaller or larger than the layer thickness (t) determined through the unaltered relation.

SEAL FOR SURGICAL INSTRUMENT

An apparatus includes a body, a shaft assembly, an end effector, a coupling member, and a seal feature. The shaft assembly extends distally from the body and includes a distal end. The coupling member is disposed at the distal end of the shaft assembly to movably couple the end effector to the shaft assembly. The seal feature is engaged with the coupling member and includes a seal body and a plurality of protrusions. The plurality or protrusions extend from the seal body. Each protrusion of the plurality of protrusions is configured to slidably receive a respective elongate member associated with the end effector therethrough.

Ultrasonic transducer techniques for ultrasonic surgical instrument

A method of fabricating an ultrasonic medical device is presented. The method includes machining a surgical tool from a flat metal stock, contacting a face of a first transducer with a first face of the surgical tool, and contacting a face of a second transducer with an opposing face of the surgical tool opposite the first transducer. The first and second transducers are configured to operate in a D31 mode with respect to the longitudinal portion of the surgical tool. Upon activation, the first transducer and the second transducer are configured to induce a standing wave in the surgical tool and the induced standing wave comprises a node at a node location in the surgical tool and an antinode at an antinode location in the surgical tool.