107 results about "Tissue Part" patented technology

The invention relates to the technical field of crop molecular genetic markers, and discloses an InDel molecular marker of avena nuda and application thereof.The molecular marker is a group of 314bp deletion variation and 2bp insertion variation in the 610439484-610440026 interval of the 5C chromosome position of a reference genome of an avena nuda variety OT3098, the nucleotide sequence of the deletion variation is shown as SEQ ID NO.1, the nucleotide sequence of the insertion variation is shown as SEQ ID NO.2, and the nucleotide sequence of the insertion variation is shown as SEQ ID NO.3. The nucleotide sequence of the insertion variation is 5 '-AA-3'. The molecular marker provided by the invention can realize stable detection in agarose gel electrophoresis by combining a specific primer pair (SEQ ID NO.2-3) with an optimized touchdown PCR (Polymerase Chain Reaction) program, has the advantage of being not influenced by a tissue part and a growth period, and provides an efficient and reliable technical means for oat germplasm identification, seed purity detection and molecular breeding.

The invention relates to a medical image processing technology, and discloses a pan cancer species histopathologic full-slice classification method and device, which is a trained multi-modal pan cancer species classification model based on histopathologic full-slice image data and full-slice diagnosis report pairing data of various tissue parts and various cancer species, and has the advantages of wide application range and high efficiency. And full slices of various pathological tissues can be classified. For classification tasks of different tissue parts, only text prompts (prompts) are used, i.e., a candidate cancer species list is set, and zero-sample full-slice classification can be realized without training. And for rare cancer species, full-slice classification can be carried out. Besides, the model has high expansibility, in order to better adapt to downstream tasks, better classification performance can be achieved by combining slice embedding with a linear classifier for use, freezing a slice embedding part and only finely adjusting the linear classifier, and the requirement for the training data size is low.

A method for sequential firings of staple cartridges is disclosed. The sequential firings including a first firing that deploys first staples into a first tissue portion from a first staple cartridge and a second firing that deploys second staples into a second tissue portion from a second staple cartridge. The method comprises monitoring a parameter indicative of a tissue response associated with the first firing, assessing the tissue response based on the parameter, and adjusting an operational parameter associated with the second firing based on the tissue response during the first firing.

A centrally coordinated and synchronized robotic system for robotic sewing procedures, such as bilateral spinal robotic sewing procedures, includes multiple robotic arms and a controller that can manipulate the robotic arms to position tools, end effectors, cameras, or navigation elements, such as a suturing needle and a marker or label for use in a robotic sewing procedure. The markers or labels may be placed on different tissue portions, including for example skin and surgically exposed tissue, to help guide the robotic arms and deployment of the markers to perform bilateral robotic sewing.

A bone displacement system includes an anchoring portion, a tool engaging portion, a compression distraction mechanism, a lateral body and a distal body. The anchoring portion has an aperture for receiving a wire to connect the anchoring portion to a proximal bone. The anchoring portion is connectable to a downwardly depending member for holding a tissue portion. The tool engaging portion is connected to the anchoring portion and is configured to connect a tool thereto. The compression-distraction mechanism is connected to the anchoring portion. The lateral body is connected to the compression-distraction mechanism and engageable with a lateral bone. The distal body is connected to the compression-distraction mechanism. The distal body has an aperture for receiving a wire to connect the distal body to a distal bone. The compression-distraction mechanism is configured to move the anchoring portion relative to the distal body.

A device for tissue shaving includes an elongated outer cannula having a tissue pinching distal end, an elongated inner shaft extending through the cannula and having a tissue shaver at a distal end. The tissue pinching distal end of the outer cannula is configured to pinch a portion of the tissue and the tissue shaver of the inner shaft is configured to be rotated and cut the pinched tissue portion via a shearing action.

The application discloses a bladder tumor specimen extractor which comprises an adjusting transmission assembly capable of controlling preliminary cutting, a separating assembly capable of separating a tissue part and a liquid part of the bladder tumor and an operating handle. The application belongs to the technical field of bladder tumor surgery. When the bladder tumor temporarily stays on a tissue liquid passing layer, the removed bladder tumor can be punctured by a plurality of groups of puncture heads, so that the tissue part of the bladder tumor is blocked by the tissue liquid passing layer, and the tissue liquid and the plasma part of the bladder tumor can pass through the tissue liquid passing layer and enter a liquid storage bag. After sampling is completed, medical staff can take out the liquid storage bag to sample the tissue liquid and the plasma part of the bladder tumor, and the tissue part of the bladder tumor can be sampled from the tissue liquid passing layer. The application provides a brand-new bladder tumor sampling experience, greatly reduces the possibility of tissue liquid and plasma remaining in the bladder and brings convenience to medical staff.

The novel pelvic and abdominal cavity drainage tube comprises a main pipeline, the main pipeline comprises a suction section and a drainage section which are connected with each other, a through suction channel is formed in the suction section in the length direction, a main channel and a plurality of auxiliary channels are formed in the drainage section in the circumferential direction, and the main channel and the auxiliary channels are through in the length direction of the suction section; the projection area of the main channel is larger than that of the auxiliary channel, and strip-shaped openings are formed in the side walls, corresponding to the drainage section, of the main channel and the auxiliary channel. The auxiliary pipeline is circumferentially provided with a plurality of drainage grooves, the outer wall of the drainage section is provided with a connecting hole corresponding to the main channel, one end of the auxiliary pipeline is inserted into the main channel along the connecting hole to enable the drainage grooves to be communicated with the main channel, drainage of the groove area of the tissue part is achieved through the auxiliary pipeline, and therefore the overall drainage range of the drainage tube is enlarged; a better drainage effect is obtained; the overall size can be reduced through connection of the auxiliary pipeline and the main channel, and therefore the wound size of the human body is reduced.

Devices for tissue treatment and fat removal are provided. In one embodiment, a device for skin tissue treatment is provided comprising: a handpiece comprising a first part configured to be positioned outside a body of a patient in proximity to a tissue portion to be treated, and a second part configured to be inserted into the body of the patient under the skin tissue surface, in proximity to or inside the tissue portion to be treated; and an RF system comprising an RF generator operable for generating RF signal and an electrode arrangement electrically coupled to the RF generator and operable for receiving the RF signal delivering RF energy to the tissue portion to cause at least one of destruction of adipose tissue cells and tissue tightening at the tissue portion, the electrode arrangement is mounted either on the first part or on the second part. In some embodiments, the second part is devoid of energy sources and gets passively heated by comprising a conductive material located inside the RF field. In some embodiments, a temperature indication system provides temperature data indicative of the temperature at the treated tissue portion.

The invention discloses a cigar tobacco tissue thickness measuring method and a cutting device, and relates to the technical field of tobacco tissue thickness measurement, and the method comprises the following steps: S1, carrying out screening treatment before cigar tobacco and rootstock cutting; s2, device cutting module selection and parameter setting work; s3, tobacco plant rhizome and leaf tissue structure slices are cut; s4, tissue slice electron microscope scanning and image selection work; and S5, carrying out tissue slice image part identification and division and average thickness calculation. The method solves the problems that in the prior art, in thickness measurement of different tissue structures of tobacco leaf sections, most methods or leaf surface image analysis systems are used for estimating and reading scale scales, and due to the fact that thickness distribution of tissue parts of leaves is not uniform and consistent, a traditional scale measurement method is large in error due to different selected measurement point positions, and the measurement accuracy is poor. And the average thickness of each part cannot be quickly and accurately measured.

The present disclosure relates to instruments, implant systems, and methods for joining bone and / or tissue portions. The instrument includes a handle portion; an inserter portion comprising an insertion portion and a tip portion; a guide portion comprising a medial end component and a distal end component, the guide portion extending from a distal end portion of the handle portion to a bone engagement end of the inserter portion; a passageway extending through the inserter portion from the distal end of the handle portion to the bone engagement end of the inserter portion; and a hole that extends from an exterior surface of the handle portion and the guide portion to the passageway, wherein the insertion portion and the tip portion of the inserter portion are positioned past the distal end component of the guide portion when the handle portion, the inserter portion, and the guide portion are mated.

The invention discloses an endoscope imaging device and method, electronic equipment and a storage medium, and relates to the technical field of image processing. The device comprises an illumination module which is used for providing an illumination light source and comprises a plurality of narrow-band light sources with different colors, and the plurality of narrow-band light sources comprise main spectral bands forming white light; the imaging module is used for imaging the reflected light after the illumination module irradiates the target part of the patient to obtain an RGB image; the processing module is used for decomposing the RGB image into a white light image and a plurality of non-white-light narrow-band images, performing enhancement processing on the plurality of non-white-light narrow-band images, and fusing the non-white-light narrow-band images with the white light image to obtain a narrow-band enhanced target image; wherein the plurality of non-white light narrow-band images respectively represent information formed by different tissue parts for absorbing narrow-band light with different wavelengths. Therefore, on the basis of a full-narrow-band illumination light source and an image decomposition-enhancement-fusion technology, the impression of white light hue is taken into consideration on the premise that focus details are highlighted through imaging.

Implant systems and related methods for joining bone and / or tissue portions is disclosed. The implant systems include a first flexible anchor tube comprising a first annular side wall defining a first internal cavity, a first longitudinal end and a second longitudinal end, and a second flexible anchor tube comprising a second annular side wall defining a second internal cavity, a first longitudinal end and a second longitudinal end. The implant systems also comprise at least one suture that passes through the first and second side walls a plurality of times. The at least one suture extends along a pattern that prevents the second anchor tube from translating along the at least one suture and allows the first anchor tube to translate along the at least one suture toward the second anchor tube when first and second end portions of the at least one suture are tensioned.

An apparatus includes a housing configured to be placed over a tissue portion of a recipient, the tissue portion overlaying an implanted device. The housing includes a cavity configured to hold a magnet therein. The apparatus further includes at least one sensor on or within the housing. The at least one sensor is configured to detect the magnet within the cavity and to generate at least one signal indicative of at least one attribute of the magnet. The apparatus further includes control circuitry within the housing. The control circuitry is configured to receive the at least one signal and, in response to the at least one signal, adjust at least one operational parameter of the apparatus.

Provided herein are suturing systems, methods of anchoring to a bone, methods for anchoring a soft tissue to a bone, and methods of anchoring a first soft tissue portion to a second soft tissue portion. An exemplary suturing system includes an anchor and a suture inserter device. The anchor includes a plurality of anchor inserts coupled to a portion of the suture between a first end and second end of the anchor. The anchor has an insertion configuration that is substantially linear and a deployed configuration that is at least partially nonlinear. The suture inserter device includes a housing comprising a housing lumen and a housing shaft disposed therein, and an inserter fork coupled to the housing shaft. The housing shaft is axially translatable, and the inserter fork is axially translatable, via the housing shaft, between a distal position and a proximal position.

The utility model discloses a clip applier. The clip applier comprises an elastic sheet fixedly arranged on a shell; the trigger is rotatably arranged on the shell so that the trigger can rotate to one of the initial position, the clamp feeding position and the clamping closing position, the clamp feeding position is located between the initial position and the clamping closing position in the rotating direction of the trigger, the elastic piece is located on the side, away from the initial position, of the trigger, and when the trigger rotates to the clamp feeding position from the initial position, the trigger abuts against the elastic piece. The elastic piece is arranged on the shell and located on the side, away from the initial position, of the trigger, and when the trigger rotates to the clamp feeding position from the initial position, the trigger abuts against the elastic piece, so that the trigger is subjected to counter-acting force in the rotating direction of the trigger, a user is reminded of force, and the user stops pressing the trigger at the clamp feeding position in time; the ligature clip can be conveniently and accurately conveyed to a surgical tissue part, so that the success rate and efficiency of the surgery are improved, the clip applier is prevented from continuously conveying the ligature clip, and the ligature clip is prevented from being wasted.

An implantable energized medical device configured to be held in position by a tissue portion of a patient, the medical device comprising: a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion extending between the first and second sides of the tissue portion, the connecting portion having a third cross-sectional area in a third plane and a third surface configured to engage the first tissue surface of the first side of the tissue portion, wherein the connecting portion is configured to connect the first portion to the second portion, wherein: the first, second, and third planes are parallel to each other, and the third cross-sectional area is smaller than the first and second cross-sectional areas, such that the first portion, second portion and connecting portion are prevented from travelling through the hole in the tissue portion in a direction perpendicular to the first, second and third planes.

To provide an endoscope for medical examination and / or treatment of a human or animal body or tissue sections thereof.SOLUTION: An endoscope (10) that is configured for imaging as well as for tissue analysis is disclosed. For this purpose, the endoscope (10) comprises an image sensor to which multiple optical devices are arranged in order to carry out different tasks with one and the same image sensor, particularly the task of imaging and measurement tasks concurrently or temporally graded.SELECTED DRAWING: Figure 1

In certain embodiments, the present disclosure provides methods of treating diseased or damaged tissue in a patient. In some forms the methods comprise introducing a photocurable composition to the diseased or damaged tissue, the photocurable composition comprising a photoactivatable metal ligand complex, a matrix forming polymer, and an electron acceptor. Such methods may further comprise irradiating the photocurable composition through a tissue portion to induce a photocrosslinking reaction forming crosslinks between individual polymers of the matrix forming polymer within the photocurable composition.

The present technology is generally directed to tissue-pexy systems including a probe and a suture thrower removably coupleable to the probe. The probe can be partially inserted into a body cavity of a patient. The suture thrower can have a tissue-receiving portion and a needle. The tissue-receiving portion can include a first concave surface defining a first recess for receiving a first tissue portion and a second concave surface defining a second recess for receiving a second tissue portion. The needle can be movable between a retracted state and an extended state. The needle can be configured to pierce through the first and second tissue portions when moving from the retracted state to the extended state. Also, the needle can be configured to pull a suture device through the first and second tissue portions when moving from the extended state to the retracted state.

A tissue closure system includes an endoscope having first and second lumens therethrough, first and second control elements disposed within the first and second lumens, respectively, and a tissue engaging portion integral with a distal end of the endoscope. The tissue engaging portion includes a tissue acquisition assembly and a tissue closure assembly. The tissue acquisition assembly is controllable via the first control element, and the tissue closure assembly controllable via the second control element. The tissue engaging portion includes a tissue grasping portion for engaging first and second target tissue portions disposed adjacent an opening in target tissue. The tissue closure assembly is configured to pierce the target tissue, and to hold the first and second target tissue portions together to close the opening in the target tissue.

The invention belongs to the technical field of medical instruments, and provides a tissue cutting tool which comprises a cutting tool shell, and a cutting device, a camera device and a clamping device are arranged on the cutting tool shell. A to-be-cut tissue part is fixed through the tissue fixing pipe, the driving mechanism drives the linkage part to achieve movement and rotation of the cutting knife body relative to the to-be-cut tissue part, so that cutting operation of the to-be-cut tissue part is achieved, meanwhile, the camera device is further arranged, a user can conveniently achieve visual operation, and the use experience of the user is improved. The clamping device can facilitate the user to adjust the position of the camera device, so that tissue cutting is completed in a stable, accurate and efficient video environment.

Provided herein are suturing systems, methods of anchoring to a bone, methods for anchoring a soft tissue to a bone, and methods of anchoring a first soft tissue portion to a second soft tissue portion. An exemplary suturing system includes an anchor and a suture inserter device. The anchor includes a plurality of anchor inserts coupled to a portion of the suture between a first end and second end of the anchor. The anchor has an insertion configuration that is substantially linear and a deployed configuration that is at least partially nonlinear. The suture inserter device includes a housing comprising a housing lumen and a housing shaft disposed therein, and an inserter fork coupled to the housing shaft. The housing shaft is axially translatable, and the inserter fork is axially translatable, via the housing shaft, between a distal position and a proximal position.

The present invention provides an implantable, energized medical device configured to be held in place by a tissue portion of a patient, the medical device comprising: a first portion configured to be positioned on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion; a second portion configured to be positioned on a second side of the tissue portion, the second side facing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion; and a connecting portion configured to be positioned through a hole in the tissue portion extending between the first side and the second side of the tissue portion, the connecting portion having a third cross-sectional area in a third plane and having a third surface configured to engage a first tissue surface on the first side of the tissue portion and configured to connect the first portion to the second portion, the first plane, the second plane, and the third plane being parallel to one another, and the third cross-sectional area being smaller than the first cross-sectional area and the second cross-sectional area, preventing the first portion, the second portion, and the connecting portion from moving through the hole in the tissue portion in a direction perpendicular to the first, second, and third planes.

The invention relates to the field of medical instruments, in particular to a repair clamp for treating valve regurgitation, a conveying device and a repair clamp detachably connected with the conveying device.The repair clamp comprises a first clamping arm, a second clamping arm and a locking mechanism, and the first clamping arm and the second clamping arm are connected and can form a clamping area; the locking mechanism comprises a restraining piece capable of being tightened, the restraining piece penetrates through the connecting structure on the repair clamp, and the restraining piece can limit relative movement of the clamping arms in the tightened state. The conveying device is detachably connected with the repair clamp and is configured to be capable of conveying the repair clamp to a target heart valve and assisting the repair clamp to be opened or closed so that a target valve leaflet tissue part can be contained in the clamping area; after being folded and used for clamping the valve leaflets, the repair clamp cannot be exposed out of the involution faces of the valve leaflets, damage caused by collision between adjacent valve leaflets and an instrument when the valve is closed is avoided, the number of the repair clamp is reduced, and the load on valve leaflet movement is relieved.

The invention relates to a method for culturing adult hair follicle protuberance cells, which belongs to the technical field of biology and comprises the following steps: S1, cleaning hair follicle tissues to obtain hair follicle tissues containing protuberance cells; s2, the hair follicle tissue containing the protuberant cells is soaked in an Advanced DMEM / F12 culture medium mixed solution containing collagenase, dispersing enzyme, EGF, bFGF and 1 * green-streptomycin, and digestion is carried out; s3, chopping hair follicle tissues containing the protuberant cells, centrifuging after stopping digestion, adding a cell culture dissociation agent into precipitated tissues, digesting twice, collecting supernatant after stopping digestion, centrifuging, collecting precipitates, re-suspending, and filtering; and S4, inoculating the cells into a cell six-well plate for 3D suspension culture, and changing the solution and blowing and beating the cells every other day. According to the method, a two-step method is adopted to digest the tissue part of the hair follicle convex cells, so that a larger number of hair follicle convex cells are obtained, and the characteristics and dryness of the hair follicle convex cells are improved.

A method of treating a patient with a bioelectrical system is provided. The method may include inserting a probe into a first position in an anatomy of the patient, the system being provided with a plurality of electrodes; energizing a first electrode of the plurality of electrodes with a measurement level of power; determining a complex impedance in the patient's anatomy; determining whether the first position is a desired position of the probe for ablating a predetermined portion of tissue of the patient, based on the complex impedance determined; and energizing one of the plurality of electrodes with an ablation level of power, the ablation level of power being greater than the measurement level of power. An apparatus for performing BIA on a patient is also provided.

A medical device includes an end effector assembly at a distal end of the medical device. The assembly comprises a pair of jaw members, a pair of electrodes including first and second electrodes, and first and second conductive wires attached to the first and second electrodes, respectively. Each jaw member includes a jaw and a tang, the jaw being transitionable between open and closed configurations for respectively receiving and collecting a tissue portion as a sample. The first and second conductive wires extend to a proximal end of the medical device and are removably connectable to a computing device configured to generate and provide electrical signals to, and determine an impedance measurement of the tissue portion based on response signals received from, the pair of electrodes contacting the tissue portion, and generate and provide a user interface indicating whether to collect the tissue portion based on the impedance measurement.

The utility model discloses a clip applier. The clip applier comprises an elastic sheet which is rotatably arranged on a shell; the trigger is rotatably arranged on the shell so that the trigger can rotate to one of the initial position, the clamp feeding position and the clamping closing position, and the rotating axis of the elastic piece is parallel to the rotating axis of the trigger. The stop rod is arranged on the trigger, the stop rod is suitable for abutting against the elastic piece to enable the elastic piece to deform in the process that the trigger rotates from the initial position to the clamp feeding position, and when the trigger rotates to the clamp feeding position, the stop rod is separated from the elastic piece to enable the elastic piece to vibrate and produce sound; in the process that the trigger rotates from the clamping position to the initial position, the stop rod is suitable for abutting against the elastic piece to drive the elastic piece to rotate so that the elastic piece can avoid the stop rod. Therefore, an obvious prompt can be given out when the clip applier conveys the clip to the forceps head, so that a user stops pressing the trigger at the clip conveying position in time, the ligature clip can be conveniently and accurately conveyed to an operation tissue part, the success rate and efficiency of an operation are further improved, the clip applier is prevented from continuously conveying the ligature clip, and waste of the ligature clip is avoided.

Graft for a bone defect, in particular a tibial head graft for a knee-joint endoprosthesis. It comprises a sleeve-like inner body (2) for implantation at one end of a long bone (99). An outer face of the inner body (2) is designed as a bone contact face (20) for bearing on the surrounding bone margin (97). According to the invention, an outer shell piece (3) is provided which, as a bone replacement piece, is doubled onto the outside of the inner body (2) for filling a defect at the cortical bone margin (97) and is not dimensioned peripherally, such that, in the circumferential direction, it covers only a part of the outer circumference of the inner body (2). The doubled outer shell piece (3) forms a filler piece for a bone defect (bone window 96) at the bone end. Closure of the bone window (96) is achieved, and unwanted contact between the graft and surrounding soft-tissue parts is avoided. Moreover, the graft is thus also supported in the region of the bone window (96). Parts of the bone margin (97) that are still present can thus remain intact, allowing the greatest possible preservation of naturally present bone substance.