A urinary output monitoring system including a urine collection assembly coupled with an automated urinary output monitoring device. The urine collection assembly includes a drainage tube, an accumulator coupled with the drainage tube, and a urine collection container fluidly coupled with the accumulator. The automated urinary output monitoring device operatively is coupled with the urine collection container. Logic determines a volume of urine collected in the container based on a signal from a load cell of the monitoring device. A vacuum pump coupled with the accumulator generates a flow of air that the drags the urine along the drainage tube to the accumulator. The accumulator separates the flow of air from the urine. The flow of air enters the drainage tube by way of a female external urinary catheter.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
A61F 5/455 - Genital receptacles for collecting urine or discharge from female member
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
3.
Weighted Gel Blanket for Targeted Temperature Management Systems
Disclosed herein a blanket apparatus and systems and methods pertaining to the same. The blanket includes a body portion formed of fabric, wherein the fabric is elastomer or elastomer-based and a first pocket within the body portion and surrounded by the fabric, wherein the first pocket is an enclosed area filled with an insulative material, and wherein the blanket is configured to be placed on at least a first thermal pad of a targeted temperature management (TTM) system, wherein the first pocket is configured to provide a weight on top of the first thermal pad. The insulative material may be an insulative gel, paste or granular material. In some instances, a length of the first pocket is substantially an entirety of a length of the blanket. Additionally, in some instances, a width of the first pocket is substantially an entirety of a width of the blanket.
A coaxial introducer cannula is provided for use with a biopsy apparatus. The coaxial introducer cannula may comprise a coaxial cannula and a hub. The hub may be fixedly attached to a proximal portion of the coaxial cannula. The hub may have a hub body, a latching lever, and a latch. The latch may be configured to rotatably engage a catch of the biopsy apparatus, and the latching lever may extend radially from the hub body. The latching lever may be longer than a height of a front plate of the biopsy apparatus so that the latching lever can be reached and rotationally operated to rotate the hub relative to the front plate of the biopsy apparatus.
A61B 10/02 - Instruments for taking cell samples or for biopsy
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
Disclosed herein is an apparatus and system directed to providing for a patient's comfort while undergoing Targeted Temperature Management (TTM). The apparatus and system pertain to a medical pad for exchanging thermal energy with a patient. The medical pad includes a flexible upper sheet, a flexible base member, an edge guard, and an adhesive surface. The flexible base member is interconnected to the flexible upper sheet to define a fluid containing layer between the flexible base member and the flexible upper sheet. The edge guard is situated along an edge of the flexible upper sheet, and extends outwardly from the edge of the flexible upper sheet. The adhesive surface is disposed on a skin-contacting side of the flexible upper sheet and the edge guard, and is adapted for releasable adhesive contact with skin of the patient.
A catheter occlusion device includes a support body configured to enclose a portion of the catheter and an inflatable member coupled to the support body. The inflatable member is in fluid communication with an inflation line. The inflatable member is configured to transition between a deflated state and an inflated state to collapse the portion of the catheter enclosed in the support body. A surface of the inflatable member can include an adhesive configured to adhere to an outer surface of the catheter. The inflatable member can include opposing first and second chambers configured to inflate toward one another to collapse the portion of the catheter enclosed in the support body.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A vacuum system can include a vacuum chamber in fluid communication with each of a catheter, a suction tube, and a fluid collecting bag. The vacuum chamber can include a proximal opening covered by a lid, a lateral opening coupled to a first drainage tube configured to receive a volume of fluid, and a distal opening coupled to a proximal opening of a valve.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
Systems and methods directed to an assisted fluid drainage system including a proximal ejector pump and a distal ejector pump coupled to a drainage tube. At least one of the proximal ejector pump and the distal ejector pump can utilize a venturi effect to move a bodily fluid through the drainage tube to prevent the formation of dependent loops, which can form within fluid drainage tubes when slack portions create a positive incline. At least one of the proximal ejector pump and the distal ejector pump can include a converging section, a diffuser section, and a diverging section. A diameter of the diffuser section can be less than a diameter of the converging section or the diverging section. A controller can be coupled to the proximal ejector pump and the distal ejector pump to initiate operation of one or both of the pumps in response to an event.
A dynamic pressure response drainage system including control logic configured to enable measuring of residual fluid disposed within the drainage lumen. The residual fluid volume is measured by detecting the magnitude of the dynamic pressure response in the system containing the residual fluid when a sudden displacement (e.g. increase or decrease) of air volume occurs inside the system. The pressure burst magnitude is related to the pressure needed to move the mass of fluid, thus the fluid volume can be calculated from measurements of the burst pressure. The magnitude of the measured air pressure exhibits a dynamic pressure response corresponding to the mass of fluid in the tube. Either positive or negative pressure bursts can be used to produce and measure the corresponding positive or negative dynamic response spike pressure.
Disclosed herein is a system, apparatus and method directed to automated adjustment of a positioning of a drainage bag based on at least an amount of tension within a tubing extending from the drainage bag. The system, apparatus and method pertain to an automated drainage bag actuation system that includes at least a first railing, a control box coupled to the first railing and configured to receive mounting fasteners that couple a drainage bag to the control box, the control box including a tension load cell sensor, a first motor, and circuitry electrically coupled to the first motor and the tension load cell sensor. The circuitry is configured to receive data from the tension load cell sensor indicating an amount of tension in tubing extending from the drainage bag and transmit one or more electrical signals to activate the first motor causing adjustment of a positioning of the drainage bag.
An apparatus and method for a fluid collection system and automated fluid flow monitoring. The system can include a urine collection container, and a detection device configured to detect a volume of fluid in the urine collection container. The detection device can be coupled to the collection container without having to compromise the integrity of the closed fluid collection system or re-catheterizing the patient. The detection device can be configured to detect an inversion event, tilt event, and the like to determine a flow rate of fluid into the container. The detection device can be communicatively coupled with external computing devices to alert a clinician when the container is nearing capacity and when it has been emptied.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A wrap assembly for a urinary catheterization procedure includes a foldable wrap body, a first plurality of urinary catheterization components and a second plurality of urinary catheterization components. The foldable wrap body can be formed of a fabric and can include a first sterile component placement area and a second sterile component placement area positioned under the first sterile component placement area. The first plurality of urinary catheterization components can be placed onto the fabric of the first sterile component placement area in a first order of use for the urinary catheterization procedure. The second plurality of urinary catheterization components can be placed onto the fabric of the second sterile component placement area in a second order of use for the urinary catheterization procedure.
A61B 50/00 - Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
Embodiments disclosed herein are fluid collection devices, and related systems and methods of use and manufacture. The fluid collection device may include a fluid impermeable barrier, a porous material, and a conduit. The fluid impermeable barrier may have an elongated shape with a proximal region and a distal region, and including a first impermeable layer and a second impermeable layer opposite to the first impermeable layer and defining an opening. The first impermeable layer and the second impermeable layer at least partially defining a chamber therebetween, the chamber including a pocket portion that extends distally from the opening between the first impermeable layer and the second impermeable layer. The porous material extends across the opening and is positioned in the pocket portion of the chamber. The porous material is configured to space the first impermeable layer from the second impermeable layer in the pocket portion of the chamber.
A case for a catheter system is disclosed, the case including a case body including a first side coupled to a second side. The case can include padding with a plurality of cavities to receive components of the catheter system and a strap to secure components of the catheter system to an interior of the case body. The case can further include one or more clips affixed to an interior wall of the first side or the second side of the case body. The one or more clips can be configured to secure additional catheter tubing or an external catheter to the interior wall of case body.
A subcutaneous tunneling device includes a shaft having a bend, a catheter connector extending from a distal end of the shaft distal of the bend, and a sleeve. The catheter connector can include a body having a gripping portion, and a barbed extension distal of the body configured for insertion into a distal opening of a catheter. The sleeve is slidably mounted on the shaft and has a retracted position exposing the catheter connector for coupling the catheter to the catheter connector via the barbed extension, and an extended position covering the catheter connector and a distal end of the catheter.
An automatic fluid flow measuring system for detecting a fluid weight change of a fluid collection system includes a load cell configured to detect a downward force and a ring connector configured to releasably couple to the load cell. The load cell can include a plate movable along a transverse axis orthogonal to a face of the plate. The plate can include a first electrical contact. The ring connector is configured to transition between an unlocked position and a locked position on the load cell. The ring connector can include a second electrical contact configured to communicate with the first electrical contact in the locked position.
F16L 37/12 - Couplings of the quick-acting type in which the connection between abutting or axially-overlapping ends is maintained by locking members using hooks, pawls, or other movable or insertable locking members
G01G 17/04 - Apparatus for, or methods of, weighing material of special form or property for weighing fluids, e.g. gases, pastes
17.
Body Fluid Input-Output Monitoring Systems and Methods
Disclosed herein is a system for monitoring the fluid balance of a patient. The system includes a fluid infusion system to deliver an infusion fluid to the patient, and a urine output (CO) system to collect and measure a UO expelled from the patient. The UO system is coupled with the fluid infusion system. A fluid input/output (I/O) logic determines fluid I/O data from fluid infusion data and CO data, rendering the I/O data on a display, and transferring I/O data to an electronic medical record. A method of monitoring a fluid balance of a patient can include: (i) calculating a fluid balance from the I/O data, (ii) comparing the fluid balance with a fluid balance limit stored in a non-transitory computer-readable storage medium, and (iii) generating an alert when the fluid balance exceeds the fluid balance limit. The method can also include generating a revised infusion order from the I/O data.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
A61M 5/14 - Infusion devices, e.g. infusing by gravityBlood infusionAccessories therefor
A61M 5/172 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters electrical or electronic
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
18.
VACUUM PORT CONNECTION FOR MEDICAL FLUID DRAINAGE SYSTEM
An embodiment of a medical fluid drainage system includes a drainage container configured to receive and hold a fluid from a patient. The drainage container is fluidly coupled and reversibly attached to a drainage bag, which receives some of fluid initially held by the drainage container. A vacuum port is provided in the drainage container for attachment to a negative pressure source. The vacuum port may be formed in a removable lid of the drainage container. The negative pressure source may remove excess air from the drainage container and drainage bag that can inflate the drainage bag and prevent fluid flow thereto.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A tissue marker is provided having a permanent portion and a biodegradable portion. The permanent portion includes a material detectable by an imaging modality. The biodegradable portion surrounds the permanent portion. The biodegradable portion includes a polymer body, a coating, and a plurality of distinct structures dispersed in the polymer body. The coating covers an outer surface of the polymer body. Each of the distinct structures include an outer shell designed to open upon the application of focused ultrasound to release a therapeutic agent within the outer shell into the polymer body. Therapeutic agents may be introduced into the biodegradable portion of the tissue marker after a period of time after introduction of the tissue marker into the tissue. In addition, methods of fabricating a three-layer tissue marker are provided.
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
Disclosed herein are urinary catheters and methods for manufacture and use. The urinary catheter can include a catheter tube, a lubricious coating over a surface of at least a distal portion of the catheter tube, and a funnel coupled to a proximal portion of the catheter tube. The catheter tube can be of a polymeric material. The lubricious coating can include a hydrophilic coating over the surface of the catheter tube and lubricant over the hydrophilic coating. The funnel can include a funnel opening in a proximal end of the funnel for voiding urine. In an example of a method of a urinary catheter, the method can include a method of making or using the urinary catheter.
A urinary drainage system can include an air pressure apparatus with a connector having an elongate connector body. The connector includes a lumen having a larger proximal lumen diameter and a smaller distal lumen diameter. The system includes an air intake adapter having an elongate adapter body, including a proximal end having a proximal opening configured to be coupled to the distal end of the connector. The adapter can include an air intake port in fluid communication with the adapter lumen, the adapter lumen having a larger proximal lumen diameter and a smaller distal lumen diameter.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 27/00 - Drainage appliances for wounds, or the like
24.
External Catheter with Finger Pocket for Self-Placement
A female external catheter includes a hollow body portion including a urethral inlet in fluid communication with an outlet. A wicking material covers the urethral inlet, and a catheter tube is coupled to the outlet, the catheter tube configured to transport urine away from the hollow body portion. The hollow body portion includes a finger portion with an opening configured to receive only a single finger to enable manipulation of the female external catheter in order to position and hold the wicking material against a urethral outlet of a female user.
A61F 5/455 - Genital receptacles for collecting urine or discharge from female member
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 25/01 - Introducing, guiding, advancing, emplacing or holding catheters
25.
Grasper and Repository for Removal of Multiple Kidney Stone Fragments
A medical instrument for insertion into and removal of kidney stone fragments from a urinary tract of a patient body includes a flexible elongate shaft coupled with a fragment retaining mechanism. The retaining mechanism can be configured to retain a plurality of fragments so that the plurality of fragments is removed from the patient with a single insertion/extraction cycle of the instrument. A fragment gathering mechanism urges fragments toward the retaining mechanism. In use, the instrument can be inserted through a working channel of a ureteroscope.
A61B 17/221 - Calculus gripping devices in the form of loops or baskets
A61B 1/307 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor for the urinary organs, e.g. urethroscopes, cystoscopes
A ureteroscope system including a ureteroscope configured for insertion into a urinary tract of a patient body is disclosed herein. The system can include an image processing module having a console with one or more processors and memory having logic stored thereon. The logic can perform various operations including providing a ureteroscope video image where transient objects have been removed to provide unobstructed visibility of persistent objects. The logic can perform other operations including object tracking, object highlighting, and object sizing. Overlays can provide for the depiction of indicia on top of ureteroscope images A method of performing a lithotripsy procedure in conjunction with the system is also disclosed.
A61B 1/307 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor for the urinary organs, e.g. urethroscopes, cystoscopes
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor
A61B 1/05 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor combined with photographic or television appliances characterised by the image sensor, e.g. camera, being in the distal end portion
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
Disclosed herein are intermittent catheters and methods thereof. In an example of an intermittent catheter, the intermittent catheter can include a catheter tube, a lubricant disposed over a surface of at least a distal portion of the catheter tube, and a funnel coupled to a proximal portion of the catheter tube. The catheter tube can be of a polymeric material. The lubricant can have a solid state below 68° F. and a liquid state above 68° F. such that the lubricant transitions into the liquid state upon insertion into a urethra of a patient or user. The funnel can include a funnel opening in a proximal end of the funnel for voiding urine. In an example of a method of an intermittent catheter, the method can include a method of making or using the intermittent catheter.
Disclosed herein is a urinary catheter assembly including a package container that is transitionable between an expanded open configuration and collapsed closed configuration having the catheter and a bag enclosed therein. The container is transitioned from the closed configuration to the open configuration in one motion by the user pulling tabs in opposite directions. The container may be sterilized along with the catheter, may define a sterile barrier and may include a tamper evident mechanism. The container is securable in the closed configuration enclosing the catheter therein before and after use of the catheter. The catheter assembly may also include a urine collection bag enclosed within the container.
An optical fiber cable is disclosed that includes an outer jacket and a plurality of cores including a first core and a second core. A plurality of channels can extend outwardly from the second core toward the outer jacket. The outer jacket can include a material doped with a photoluminescent material configured to absorb energy from light propagating along the second core causing photoluminescence. The optical fiber cable may include cladding surrounding the first and second cores and the plurality of channels. The first core may propagate a first laser beam having wavelength of substantially 1940 nanometers while the second core and the plurality of channels may propagate a second laser beam having a wavelength of within the range of 360-830 nanometers. A system for providing a medical treatment including a first medical instrument optically coupled to the optical fiber cable is also disclosed.
A61B 18/22 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibreHand-pieces therefor
A61B 17/00 - Surgical instruments, devices or methods
A61B 18/00 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
G02B 6/036 - Optical fibres with cladding core or cladding comprising multiple layers
A medical instrument is disclosed that includes an elongate flexible shaft, a plurality of optical fibers extending along the length, and a laser control module coupled with the optical fibers. The instrument is configured for insertion into a patient body and/or into a working channel of an endoscope (e.g., ureteroscope). The instrument is configured for ablation of body tissue and/or a foreign substance within the body. The optical fibers can define a cross-sectional diameter within a range of 50 μm to 150 μm. Three or more of the optical fibers can be bundled together defining a circumscribed circle having a cross-sectional diameter less than 500 μm. Some optical fibers are peripherally disposed along the shaft and are configured to direct light radially outward. A lumen extending along the length of the shaft is coupled with fluid port coupled with the shaft.
A61B 18/26 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibreHand-pieces therefor for producing a shock wave, e.g. laser lithotripsy
A61B 18/22 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibreHand-pieces therefor
31.
Catheterization System and Methods for Use Thereof
A catheterization system including a catheter, drainage bag and one or more indicators configured to measure an attribute relating to the usage of the catheter system and communicate information about the attribute to a network, such as an Electronic Medical Record (EMR) database. The indicators may include a location indicator, a duration indicator, an elevation indicator, a tamper indicator, a dependent loop indicator, a floor contact indicator, and a patient securement indicator. The system may autonomously detect and record one or more attributes relating to the usage of the catheter system.
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
32.
Package and Method of Use for Managing Excess Laser Fiber
Disclosed herein is a laser fiber surrounded by tubular package, the tubular package having a plurality of sections along a length of the tubular package, each of the plurality of sections connected to an adjacent section by a circumferential tear line, each of the plurality of sections including a length marking.
B65D 85/04 - Containers, packaging elements or packages, specially adapted for particular articles or materials for annular articles for coils of wire, rope or hose
B65D 85/20 - Containers, packaging elements or packages, specially adapted for particular articles or materials for incompressible or rigid rod-shaped or tubular articles
A fluid collection device includes a fluid collection container and an adapter. The fluid collection container includes a vent. The adapter is configured to removably couple with the fluid collection container over the vent. The adapter includes a connecting portion and a port attachable to the connecting portion. The port has a non-sealed position and a sealed position with respect to the vent when the connecting portion is coupled to the fluid connection container and positioned over the vent. In the non-sealed position the vent is in fluid communication with a surrounding environment.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
Disclosed herein is an endoscope imaging system including an endoscope configured to capture one or more images, the endoscope in communication with a laser system and a display, and a console, in communication with the endoscope, the laser system and the display, the console configured to receive one or more parameter settings from the laser system, receive the one or more captured images from the endoscope, generate one or more icons corresponding to the parameter settings and overlay the icons on the captured images depicted on the display.
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor
A61B 17/00 - Surgical instruments, devices or methods
35.
Physician Enabled Laser Control from Ureteroscope Handle
A system for providing a medical treatment, including a first medical instrument and a second medical instrument is disclosed. The first medical instrument includes a first operator interface configured to define a plurality of operating parameters of the first medical instrument. The second medical instrument includes a second operator interface configured to define a subset of the plurality of operating parameters. The first operator interface is configured for placement and use outside of a sterile field and the second operator interface is configured for placement and use within the sterile field. The second operator interface is attached to or attachable to a handle of the second medical instrument. The handle is configured for manipulation by a hand of the operator and the second operator interface is configured for interaction with one or more extremities of the same hand.
A61B 34/00 - Computer-aided surgeryManipulators or robots specially adapted for use in surgery
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor
A61B 1/307 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopesIlluminating arrangements therefor for the urinary organs, e.g. urethroscopes, cystoscopes
A61B 17/00 - Surgical instruments, devices or methods
A61B 18/00 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
A61B 18/26 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibreHand-pieces therefor for producing a shock wave, e.g. laser lithotripsy
An intermittent catheter package including a plurality of components and a catheterization tray configured to facilitate a catheterization procedure. The plurality of components include a urinary catheter fluidly connected to a urine-drainage bag and a sampling-port access device configured to fluidly connect to a urine-sampling port of the urinary catheter or the urine-drainage bag for aseptic collection of one or more urine samples.
An intermittent catheter package including a plurality of components and a catheterization tray configured to facilitate a catheterization procedure. The plurality of components include a urinary catheter fluidly connected to a urine-drainage bag and a sampling-port access device configured to fluidly connect to a urine-sampling port of the urinary catheter or the urine-drainage bag for aseptic collection of one or more urine samples.
The catheterization tray includes at least a first compartment, a second compartment, a third compartment, and a fourth compartment. The second compartment is connected to the third compartment Step-by-step surface instructions for performing the catheterization procedure are incorporated into the catheterization tray.
A61B 50/00 - Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
Disclosed herein is a urinary catheter-insertion kit for a catheterization procedure. The urinary catheter-insertion kit can include a tray assembly, a urinary catheter, and a drainage system. The tray assembly can be contoured for a space between partially opened legs of a patient. The tray assembly can include a storage tray and a working tray. The working tray can include a number of preformed sections holding a number of components of the urinary catheter-insertion kit. The working tray can be suspended over the storage tray in the tray assembly, thereby forming a covered storage space in the storage tray. The urinary catheter can be disposed in a catheter section of the preformed sections of the working tray. The drainage system can be disposed in the storage space. The drainage system can include a drainage receptacle and drainage tubing connected to the urinary catheter.
Surgical fasteners for use with articulating surgical instruments are disclosed. In one embodiment, a surgical fastener may include a head, a shaft extending distally from the head, and a through bore extending through the shaft from a proximal surface of the head to a distal end of the shaft. A fastener carrier of a surgical instrument may be slidably received in the through bore, and the through bore may be sized and shaped to have two or fewer contact points with the fastener carrier when the fastener carrier is in a fully articulated configuration. In another embodiment, a fastener may include a head, a shaft extending distally from the head and including a distal tip, a sloped surface sloping toward the distal tip, and a through bore passing through the head, shaft, and sloped surface. The sloped surface may terminate at two shoulders located on opposing sides of the through bore.
A61B 17/88 - Methods or means for implanting or extracting internal fixation devices
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
A repair prosthetic for repairing a hernia is disclosed. In some embodiments, the repair prosthetic includes a patch body, a frame that assists in spreading the patch body from a reduced configuration to an expanded configuration, and a plurality of tethers attached to the patch body at locations between the frame and a periphery of the patch body. In various embodiments, the tethers can be tensioned to mitigate curling or creasing in the patch body to flatten the patch to facilitate attachment to tissue.
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
A61B 17/06 - NeedlesHolders or packages for needles or suture materials
A securement device holds a medical article having flexible portions in position upon the body of a patient and inhibits movement of the medical article. The medical article may be insertable into the securement device from above from below or along a longitudinal axis of the device. The securement device may have abutment surfaces which interact with the flexible portions of the medical article to further inhibit rotation of the device. A securement kit can include a securement device and a catheter.
Urinary catheter kits can include a working tray, a storage tray, a protective paperboard, and a urinary catheter assembly, including a urinary catheter and a drainage system. The working tray can be nested on top of the storage tray. The working tray can include preformed sections configured to accommodate a plurality of components of the urinary catheter kit.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
Articulating surgical instruments are disclosed. In one embodiment, a surgical instrument may include an elongated shaft assembly including an articulable portion moveable between a non-articulated configuration and an articulated configuration. First and second articulating shafts of the elongated shaft assembly may be coaxially arranged and axially fixed at an attachment point located distally from the articulable portion. Proximal portions of the first and second articulating shafts may be displaceable in opposing directions to articulate the articulable portion from the non-articulated configuration to the articulated configuration. In another embodiment, an articulation control may be movable from a first position to a second position to move an articulation lock from a locked configuration to an unlocked configuration to selectively permit articulation of a surgical instrument. The articulation lock also may be movable from the second position to a third position to articulate the surgical instrument.
A61B 17/04 - Surgical instruments, devices or methods for closing wounds or holding wounds closedAccessories for use therewith for suturing woundsHolders or packages for needles or suture materials
A61B 17/10 - Surgical instruments, devices or methods for closing wounds or holding wounds closedAccessories for use therewith for applying or removing wound clampsWound clamp magazines
A61B 17/29 - Forceps for use in minimally invasive surgery
(1) Surgical and medical devices and instruments; surgical and medical devices and instruments, namely, medical and surgical lasers; surgical and medical devices and instruments, namely, pulse generators; surgical and medical devices and instruments with embedded operating system software; laser fibers for medical and surgical purposes, and parts and fittings therefor
44.
Catheter Insertion Device Including Top-Mounted Advancement Components
A catheter insertion device includes a housing, a needle coupled to a needle hub, a catheter pre-disposed over the needle, a guidewire pre-disposed in a lumen of the needle, a guidewire advancement assembly configured to distally advance the guidewire with respect to the needle, and a catheter advancement assembly configured to distally advance the catheter with respect to the needle. The needle hub can be fixed to an interior of the housing with a distal section of the needle extending from the housing. The catheter advancement assembly can include a tail portion to engage the needle hub in order to prevent movement of the catheter advancement assembly. The catheter insertion device can also include a flash indicator with an elongate channel in fluid communication with the needle lumen. The elongate channel can include a viewable pathway to indicate to a user that the needle tip is within a blood vessel.
A method of making an elongate catheter tube, includes forming an outer surface with opposing flat sides, forming a first lumen with a first cross-sectional circular shape and a first cross-sectional area, forming a second lumen with a second cross-sectional circular shape and a second cross-sectional area substantially equivalent to the first cross-sectional circular shape and the first cross-sectional area, and forming a third lumen with a third cross-sectional circular shape and a third cross-sectional area. The third cross-sectional area can be smaller than the first cross-sectional area and the second cross-sectional area. The third lumen can be axially offset from a central axis of the elongate catheter tube and adjacent to a first side of the opposing flat sides. The third lumen can be formed to withstand pressures associated with power injection of a fluid therethrough.
A61M 1/36 - Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation
A61M 5/00 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular wayAccessories therefor, e.g. filling or cleaning devices, arm rests
B29C 48/11 - Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels comprising two or more partially or fully enclosed cavities, e.g. honeycomb-shaped
B29C 48/12 - Articles with an irregular circumference when viewed in cross-section, e.g. window profiles
B29K 75/00 - Use of polyureas or polyurethanes as moulding material
A system is disclosed for recommending a thermal pad set for use in providing a targeted temperature management (TTM) therapy to a patient, where the system includes a computer implemented method. The computer implemented method includes receiving a request for a thermal pad set recommendation from a clinician device, receiving a patient's identification from the clinician device, retrieving one or more patient parameter values from an electronic medical record for the patient, determining a pad set recommendation according to the patient parameter values in combination with a pad set correlation table, and displaying the pad set recommendation on the clinician device. Also disclosed herein is a system including a non-transitory computer-readable medium with instructions encoded thereon and one or more processors configured to, when executing the instructions, perform operations in accordance with processes of the computer implemented method.
A61F 7/08 - Warming pads, pans or matsHot-water bottles
A61F 7/00 - Heating or cooling appliances for medical or therapeutic treatment of the human body
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
G16H 20/30 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
G16H 50/70 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
Disclosed herein are female external catheters (“FECs”) and methods thereof. For example, an FEC can include a catheter body, a catheter back, and a connector. The catheter body can include a cavity extending along a length of the catheter body. The cavity is configured to open toward a patient. The catheter back can include a connector hole aligned with an end portion of the cavity. The connector hole can be configured to open away from the patient. The connector is disposed in the connector hole. The connector can include a sump configured to collect urine from the end portion of the cavity for withdrawal from the FEC. In another example, a method of an FEC can includes a method of using the FEC.
A61F 5/455 - Genital receptacles for collecting urine or discharge from female member
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
Disclosed herein is a medical device projection system. The medical device projection system includes a first medical device outside of a sterile field, the first medical device having a user control interface including a plurality of parameters. The medical device projection system further includes a projector within the sterile field, the projector in communication with the first medical device and configured to project a mixed reality visual representation of the user control interface on a surface.
A61B 34/00 - Computer-aided surgeryManipulators or robots specially adapted for use in surgery
A61B 18/20 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser
A61B 46/23 - Surgical drapes specially adapted for patients with means to retain or hold surgical implements
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
49.
Systems and Methods for Hyperthermic Cancer Treatment
Disclosed are systems and methods for hyperthermic cancer treatment. For example, a system can include a heat exchanger, a control module, a primary fluid delivery line (“FDL”), an intravenous catheter, and a peristaltic pump. The control module can include at least a hydraulic system configured to provide a temperature-controlled fluid. The primary FDL can be configured to convey the temperature-controlled fluid to the heat exchanger as a supply fluid and back to the hydraulic system as a return fluid. The intravenous catheter can include a primary lumen configured to convey blood of the patient to the heat exchanger as well as a secondary lumen configured to convey the blood back to the patient using the peristaltic pump. The catheter can also include a thermistor for determining a core body temperature of the patient to ensure the patient is in a hyperthermic state before administering a cancer treatment to the patient.
Disclosed herein is a medical system including an equipment module, a limited use device, and a functional interface configured to operatively couple the limited use device with the equipment module via a non-proprietary connector. The equipment module includes an identification interface configured to obtain identification data from the limited use device, and the equipment module is configured to modify operation of the system in accordance with a result of obtaining the identification data. A method of operation includes disabling operating features if the brand of the limited use device is different from the brand of the equipment module. Computer logic and a computerized method include detecting coupling of an equipment module to a console and attempting to obtain identification data of the equipment module. As a result, the console enables either a first set or a second set of operations.
G16H 40/40 - ICT specially adapted for the management or administration of healthcare resources or facilitiesICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
Medical devices and apparatus, namely, stents, covered stents, stent delivery systems and parts and fittings therefor; Medical and surgical instruments to treat peripheral artery disease.
(1) Medical devices and apparatus, namely, stents, covered stents, stent delivery systems and parts and fittings therefor; medical and surgical instruments to treat peripheral artery disease
Disclosed herein is an apparatus and system directed to providing for a patients comfort while undergoing Targeted Temperature Management (TTM). A medical pad with the TTM can include a flexible upper sheet, a flexible base member, an adhesive surface, and an edge guard. The flexible base member can be interconnected to the flexible upper sheet to define a fluid containing layer including a plurality of tortuous fluid flow paths. The adhesive surface can be disposed on a skin-contacting side of the flexible upper sheet, and can be adapted for releasable adhesive contact with skin of the patient. The edge guard can include a pliant shock-absorbent material surrounding a portion of an edge of the flexible upper sheet, and can be configured to distribute pressure from the medical pad across a portion of the patients body in contact with a surface of the edge guard.
A urinary catheter and container. The urinary catheter can include a catheter shaft attached to a handle and a coating disposed on an outer surface of the catheter shaft. The coating can include a hydrogel, water and/or glycerin, and a polyethylene gylcol (PEG). The PEG can have a molecular weight equal to or less than 600, for example one or more of polyethylene glycol (PEG) 300 and PEG 400. The coating can be applied in a wet state and remain wet for an extended period of time in the container, thereby obviating the need for a lubricant, such as a water sachet or gel package, to accompany the catheter in the container. The container can include a gas impermeable foil material. The container can include an adhesive tab covering a perforated section, the adhesive tab including a pull loop.
A catheterization package including a catheterization tray and contents for a catheterization procedure. The catheterization tray can include a structural configuration for maintaining a sterile field about a patient throughout the catheterization procedure, the sterile field including at least a portion of the tray. The structural configuration of the tray can provide a sterile side of the tray designated for a first person performing sterile steps of the catheterization procedure in the sterile field. The structural configuration of the tray can also provide a non-sterile side of the tray designated for either the first person or a second person performing non-sterile steps of the catheterization procedure outside the sterile field. The contents for the catheterization procedure can include a perineal care kit, two or more pairs of gloves, and a drainage system including a catheter.
An automated urine-output-measurement system can include single-patient equipment and/or multi-patient equipment. The single-patient equipment can include a urinary catheter and a urine-collection system. The urine-collection system can include drainage tubing and a drainage receptacle. The multi-patient equipment can include a urine monitor. The urine monitor can include a housing having a cavity configured to completely encompass the drainage receptacle, a urine measurement device configured to measure urine output into the drainage receptacle, and an integrated display screen configured to display patient information including measurements of the urine output. A method of the automated urine-output-measurement system can include placing the drainage receptacle in the urine monitor of the automated urine-output-measurement system, and confirming a volume of urine in the drainage receptacle with that indicated on the urine monitor once a patient has produced urine.
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
Medical devices and apparatus, namely, stents, covered stents, stent delivery systems and parts and fittings therefor. Medical and surgical instruments to treat peripheral artery disease.
Embodiments disclosed herein are directed to apparatus and methods for automatic fluid flow system connectors. The system generally includes a load cell interface coupled to a console and a ring connector coupled to a fluid collection system. The ring connector can be releasably engaged with the load cell using an engagement structure such as a latch, locking arm, or spring clip mechanism. The ring connector and load cell can include electrical contacts configured to engage along an axis that extends perpendicular to a surface that the electrical contacts are disposed on. Advantageously, reduced wear on the electrical contacts should extend the usable life of the system.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
G01F 23/20 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measurement of weight, e.g. to determine the level of stored liquefied gas
G01G 17/04 - Apparatus for, or methods of, weighing material of special form or property for weighing fluids, e.g. gases, pastes
G01G 19/18 - Weighing apparatus or methods adapted for special purposes not provided for in groups for weighing suspended loads having electrical weight-sensitive devices
An intermittent catheter package including a plurality of components and a catheterization tray configured to facilitate a catheterization procedure. The plurality of components include a urinary catheter fluidly connected to a urine-drainage bag and a sampling-port access device configured to fluidly connect to a urine-sampling port of the urinary catheter or the urine-drainage bag for aseptic collection of one or more urine samples. The catheterization tray includes at least a first compartment, a second compartment, and a third compartment configured to hold the plurality of components. The first compartment is configured to hold the urinary catheter. The second compartment is connected to the first compartment by an intercompartment connection. The second compartment is configured to hold the urine-drainage bag. The third compartment is configured to hold the sampling-port access device. Step-by-step instructions are incorporated into the catheterization tray to facilitate the catheterization procedure.
B65B 5/02 - Machines characterised by incorporation of means for making the containers or receptacles
B65B 5/08 - Packaging groups of articles, the articles being individually gripped or guided for transfer to the containers or receptacles
B65D 77/20 - Container closures formed after filling by applying separate lids or covers
A61B 50/00 - Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
Disclosed herein are systems and methods for providing targeted temperature management (TTM) therapy to a patient. For example, TTM systems can include rotatable connector systems for coupling a fluid deliver line to a thermal contact pad. Embodiments of the connector system can include connector pairs that comprise one lumen or multiple lumens. The TTM system includes embodiments where a second thermal pad is coupled to a first thermal pad.
Disclosed herein are systems and methods for providing targeted temperature management (TTM) therapy to a patient. For example, TTM systems include a connection system for coupling a fluid deliver line to a thermal contact pad. The connection system is configured to provide indication to the user that the fluid deliver line is completely connected to thermal contact pad. In addition, the connection system also includes a controller for activating a connection lock and for sharing signals with a TTM system module. The fluid deliver line includes a pair of conduits arranged concentrically and the thermal pad includes a TTM fluid filter disposed within a fluid containing layer.
Embodiments disclosed herein are directed to a self-learning bladder volume monitoring system. The system can include a bladder volume (BV) system configured to measure an electrical impedance of a bladder region of a patient and determine a volume of fluid disposed therein using an impedance to bladder volume model (“By model”). Further, the system can measure a total body water (“TBW”) for the patient and modify the BV model to account for variations in TBW within the tissues surrounding the bladder providing a more accurate bladder volume measurement. The system can include a “training unit” which can include one of a user input interface, an automatic urine output monitoring system, an ultrasound system, and an intrabladder pressure system configured to verify a volume of fluid within or voided from the bladder and train the BV model.
Medical and surgical sealants; Medical and surgical sealants, devices, and plugs for use in biopsies; Medical and surgical sealants, devices, and plugs for oncology applications.
65.
Targeted Temperature Management Systems, Pads, and Methods Thereof
Disclosed herein are systems, pads, and methods thereof for targeted temperature management. A system, for example, can include a control module and a pad. The pad can include a multilayered pad body and one or more comfort-enhancing features integrated into the pad for mitigating or eliminating skin irritation along at least edges of the pad. The multilayered pad body can include a conduit layer, an impermeable film over the conduit layer, and an adherable layer over the impermeable film. The conduit layer can include one or more conduits configured to convey a fluid through the conduit layer. The impermeable film can be configured to retain the fluid in the conduit layer when the fluid is conveyed through the conduit layer. The adherable layer can be configured to adhere to a body portion of a patient. Methods of the systems and pads can include methods of use.
Disclosed herein are systems and methods for providing targeted temperature management (TTM) therapy to a patient. The TTM system can include multiple embodiments of a thermal pad including embodiments that are convertible from a first patient contact area to a second patient contact area. Embodiments of thermal pads can include pads that are expandable, extendable, and/or comprise attachable or removable portions. The TTM system can include embodiments where a second thermal pad is coupled to a first thermal pad.
An intraosseous access device can include a device body, a trocar needle coupled to the device body, and an intraosseous catheter removably disposed on the trocar needle. The device body can be configured to enable manual insertion of a distal tip of the trocar needle through a skin surface of a patient to an external surface of a bone of the patient. The intraosseous catheter can include a catheter hub and a cannula slidable with respect to the catheter hub to enable adjustment of a longitudinal length of the intraosseous catheter. The intraosseous access device can further include an advancement mechanism configured to advance the trocar needle and the intraosseous catheter into an internal portion of the bone after the distal tip of the trocar needle and the intraosseous catheter have been inserted through the skin surface of the patient to the external surface of the bone of the patient.
Embodiments disclosed herein are directed to a dynamic pressure response system for fully automated clearing of dependent loops from a fluid drainage system. Fluid drainage systems include a flexible drainage tube providing fluid communication with a collection container. Dependent loops can form within the tube leading to pooling of urine and provide an increased risk in CAUTI. Dynamic pressure response systems can automatically detect the presence of dependent loops and provide a low-rate positive air pressure to clear the columnized fluid. Further, the system can automatically detect mixed fluid states when a noise level of pressure signals increases, the system can then provide high-rate positive air pressure to clear mixed fluid state liquid from the tube lumen.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilitiesICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
69.
Apparatus and Methods Relating to Intravascular Positioning of Distal End of Catheter
Systems and methods for navigation and positioning a central venous catheter within a patient. The system may include a first pole and a second pole designed to generate an electric field sufficient to obtain a plurality of field measurements. The system may include a stylet inserted into a medical device. The stylet may include a magnetic assembly configured to produce a magnetic field positioned along a distal portion of the stylet, and a stylet electrode positioned distal of the magnetic assembly. The stylet electrode may be designed to function as both an interior excitation electrode and an interior detection electrode. Advancement of the medical device in the patient may include using a conductance curve generated from the plurality of field measurements to identify an obstruction or malposition in the patient.
A surgical instrument including a power assist device, and its method of use for deploying surgical fasteners, is disclosed. The surgical instrument may include a handle, an elongated shaft extending from the handle, and a surgical fastener deployment system including a driveshaft. The driveshaft is actuatable between at least a first proximal position and a second distal position. A striker is movable relative to the driveshaft and an impact surface is associated with the driveshaft. The impact surface is constructed and arranged to be struck by the striker member to displace the driveshaft to the second distal position and deploy the surgical fastener.
A61B 17/10 - Surgical instruments, devices or methods for closing wounds or holding wounds closedAccessories for use therewith for applying or removing wound clampsWound clamp magazines
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
71.
Catheter Assembly Including Monitoring Capabilities
A catheter assembly or other elongate tubular device for use in establishing vascular or other access within the body of a patient is disclosed. The catheter assembly is equipped with one or more sensors that enable monitoring of one or more physiological aspects of the patient or physical aspect of the catheter assembly itself when the catheter assembly is disposed within the patient. Such aspects include central venous pressure, body temperature, ECG heart signals, oxygen levels, ultrasound data, glucose, etc. The catheter assembly includes the ability to wirelessly transmit or otherwise forward data relating to the detected physiological parameters to another location, such as a patient electronic medical record, smartphone or other mobile device, nurse station, etc. Catheter assemblies configured to detect the frequency of catheter flushing, flushing quality, etc., are also disclosed.
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilitiesICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
Medical device kits for use in placing, maintaining, altering, and/or removing medical devices in, on, and/or from the body of a patient can include one or more wrap assemblies for use in the placement/maintenance procedure. The one or more wrap assemblies of the medical device kit can include various features to assist the clinician performing the particular procedure, such as a urinary catheterization procedure. A wrap assembly can include a wrap body including a front surface defining an aseptic field for the urinary catheterization procedure, a plurality of pockets on the front surface, and urinary catheterization components disposed in the plurality of pockets, the urinary catheterization components arranged in a predetermined order of use for the urinary catheterization procedure. The wrap assembly can be in a rolled configuration. A method of using the wrap assembly includes unrolling the wrap assembly and removing the urinary catheterization components to perform the procedure.
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
A guidewire comprising a hydrophilic surface coating encasing a core and a metal coil along a longitudinal length of the hydrophilic surface coating to form a distal closed tip, the metal coil circumscribing the core along a predetermined length, the core extending longitudinally beyond the metal coil in both a proximal direction and a distal direction, wherein a proximal section of the guidewire includes a hydrophobic surface coating.
An endovascular implant for forming a fistula includes a body including a wall forming a lumen having a distal opening and a proximal opening. An anchor is coupled to a distal end of the body adjacent the distal opening. The anchor may include a first anchor extending from a first side of a distal end of the body, and a second, separate anchor may extending from a second side of the distal end of the body. A retriever may be coupled to a proximal end of the body adjacent the proximal opening.
Disclosed are laser modules for laser systems and methods thereof that expand options for clinicians when using lasers in medical procedures such as holmium lasers in urological procedures. A laser module includes independently drivable laser-producing assemblies, laser optics, and a driver for driving the laser-producing assemblies. Each laser-producing assembly includes an optical resonator having a gain medium set among resonator optics for directing light through the gain medium for amplification of the light by stimulated emission. The laser optics combines two or more input laser beams produced by the laser-producing assemblies into a combined laser beam having a pulse energy, a pulse width, or a pulse repetition frequency resulting from a combination of the two-or-more input laser beams. The laser optics also directs at least a portion of the combined laser beam through an outlet of the laser module as an output laser beam.
H01S 3/23 - Arrangement of two or more lasers not provided for in groups , e.g. tandem arrangement of separate active media
H01S 3/10 - Controlling the intensity, frequency, phase, polarisation or direction of the emitted radiation, e.g. switching, gating, modulating or demodulating
H01S 3/091 - Processes or apparatus for excitation, e.g. pumping using optical pumping
76.
Application of Antimicrobial Agents to Medical Devices
Invasive medical devices including a substantially non-eluting antimicrobial treatment. One or more external and/or internal surfaces of the medical device include a substantially non-eluting copper-coated surface that assists in preventing microbial colonization of the coated surface. This in turn reduces the incidence of infection to the patient originating from the medical device. In one embodiment, a catheter assembly is disclosed and comprises an elongate catheter tube that defines at least one lumen, at least one extension leg including a luer connector, and a bifurcation hub including at least one fluid passageway that provides fluid communication between the extension leg and the lumen. A substantially non-eluting copper coating is disposed on a surface of at least one of the lumen, the extension leg, the luer connector, and the fluid passageway. The coating is applied via an electroless deposition process. A water-shed coating is disposed on the copper coating.
A fluid control component configured for controlling fluid flow through the hub of a catheter assembly during and after placement into the patient is disclosed. In one embodiment, the fluid control component comprises a body disposed within a cavity of the hub, the body being movable between a first position and a second position, wherein the body does not pierce a valve disposed in the hub when in the first position and wherein the body pierces the valve when in the second position. The body includes a conduit to enable fluid flow through an internal portion of the body when the body is in the second position, and a plurality of longitudinal ribs disposed on an exterior surface of the body. The longitudinal ribs can provide fluid flow channels between the valve and an external portion of the body when the body is in the second position.
Provided herein is a catheter assembly including, in some embodiments, a core wire configured for linear actuation and a damping mechanism around the core wire. The core wire includes a proximal end with a sonic connector configured to couple to an ultrasound-producing mechanism. The core wire includes a distal end configured to modify intravascular lesions with vibrational energy from the ultrasound-producing mechanism. The damping mechanism includes a gasket system and a retainer to retain the gasket system in a damping-mechanism bore of the catheter assembly. The damping mechanism is around a proximal-end portion of the core wire, where the damping system can provide a compressive force sufficient to dampen transverse wave-producing vibrational energy in the proximal-end portion of the core wire without restricting the linear actuation of the core wire through the damping mechanism including extension and retraction of the core wire through the damping mechanism.
A61B 17/22 - Implements for squeezing-off ulcers or the like on inner organs of the bodyImplements for scraping-out cavities of body organs, e.g. bonesSurgical instruments, devices or methods for invasive removal or destruction of calculus using mechanical vibrationsSurgical instruments, devices or methods for removing obstructions in blood vessels, not otherwise provided for
79.
Catheter insertion tray with integrated instructions
An improved medical procedure or catheterization tray included in an improved medical procedure or catheterization package. The improved medical procedure or catheterization tray is intuitively arranged. In one example, a catheterization package and catheterization tray has a layout and/or arrangement of components that may help reduce CAUTI rates by facilitating ease of use and aiding in proper aseptic technique during insertion. The medical procedure or catheterization package and/or medical procedure or catheterization tray may include various implements, compartments, and components necessary and/or helpful to the medical procedure or catheterization.
A61B 50/00 - Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
A61B 50/20 - Holders specially adapted for surgical or diagnostic appliances or instruments
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
A61M 5/00 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular wayAccessories therefor, e.g. filling or cleaning devices, arm rests
A device for introduction into a body vessel includes a shaft, a balloon positioned at the distal end of the shaft, a guidewire disposed longitudinally within the shaft to receive a guidewire during use, a balloon disposed at the distal end of the shaft, and longitudinal scoring wires to score a vascular lesion attached to the distal end of the shaft, disposed over the balloon and disposed within the shaft. The proximal ends are welded or otherwise affixed to a spring mounted in the handle. The balloon expands when fluid is delivered to the balloon through the inflation lumen. This expansion pushes the scoring wires against the vascular lesion.
A61B 17/22 - Implements for squeezing-off ulcers or the like on inner organs of the bodyImplements for scraping-out cavities of body organs, e.g. bonesSurgical instruments, devices or methods for invasive removal or destruction of calculus using mechanical vibrationsSurgical instruments, devices or methods for removing obstructions in blood vessels, not otherwise provided for
An antimicrobial catheter assembly can include a non-eluting antimicrobial coating on an internal surface, an external surface, or both the internal surface and the external surface of the catheter assembly. The antimicrobial coating can be a composite of three or more layers including a copper-based layer between an outer corrosion-preventing layer of a corrosion-resistant metal and an inner adhesion promoting layer.
Surgical instruments and their methods of use are described. In one embodiment, a surgical instrument includes a power transmission including a trigger and a fastener driver operatively coupled to the trigger. Actuation of the trigger from a first configuration to a second configuration moves the fastener driver between at least a first position and a second position. Additionally, an actuation lockout system operatively associated with the power transmission is moveable between a locked configuration and an unlocked configuration. The actuation lockout system prevents movement of the fastener driver from the first position to the second position when the actuation lockout system is in the locked configuration. Actuation of the trigger from the first configuration towards the second configuration moves the actuation lockout system from the locked configuration to the unlocked configuration.
A61B 17/29 - Forceps for use in minimally invasive surgery
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
83.
Intermittent-Catheter Assembly and Methods Thereof
An intermittent-catheter assembly (100) includes an intermittent catheter and a catheter housing (102). The intermittent catheter includes a funnel and a catheter tube fluidly coupled to the funnel. The catheter housing (102) includes the intermittent catheter disposed in the catheter housing while in a packaged state of the intermittent-catheter assembly. The catheter housing includes an inner sleeve (104) and an outer sleeve (102). The inner sleeve (104) includes a longitudinal cavity containing a majority of the intermittent catheter in the packaged state of the intermittent-catheter assembly. The outer sleeve (106) is slidably disposed over the inner sleeve (104). The catheter housing (102) is configured to expose the intermittent catheter for removal from the catheter housing (102) when the outer sleeve (106) is grasped and slid toward an exposed end of the inner sleeve (104) in opposition to a force applied to the exposed end of the inner sleeve (104).
A medical balloon includes a base balloon layer and at least one cellulose fiber applied to the base balloon layer, such as by an adhesive. The cellulose fiber may include hydro-dynamically focused, cellulose nano fibers. The cellulose fiber may be a longitudinal fiber extending along the base balloon substantially parallel to the longitudinal axis, at least one hoop fiber over the at least one longitudinal fiber, or both, including possibly as a single continuous fiber. The at least one fiber may further include silk proteins, and at least one silk fiber may also be included. An outer layer, such as a polymer film or spray coating, may be applied over the at least one cellulose fiber. Related methods are also disclosed.
Medical and surgical sealants in the nature of surgical sealants being plugs to seal punctures for use in needle and surgical biopsies; Medical and surgical devices for use in needle and surgical biopsies, namely, kits comprising syringes for medical purposes, needles for medical purposes, stylets for medical purposes, mixing clips for medical purposes, and medical stylet applicators; Medical and surgical plugs to seal punctures and devices for use in oncology, namely, kits comprising syringes for medical purposes, needles for medical purposes, stylets for medical purposes, mixing clips for medical purposes, and medical stylet applicators
86.
RE-ENTRY DEVICE FOR VESSEL RECANALIZATION USING A SUBINTIMAL TECHNIQUE
A re-entry device for recanalization of a vessel using a subintimal technique. A catheter (10) includes a first inner lumen (14) extending to a distal end portion (12b) of the catheter, the distal end portion including an angled tip (20) having a distal open end (20a). An elongated stylet (24) is located in the first inner lumen, the stylet having an angled distal end portion (24a) forming a needle. An actuator (26) at a proximal end portion (12a) of the catheter is for advancing the stylet from a retracted position within the catheter to a deployed position projecting from the distal open end of the angled tip for penetrating a wall of the vessel.
A61B 17/22 - Implements for squeezing-off ulcers or the like on inner organs of the bodyImplements for scraping-out cavities of body organs, e.g. bonesSurgical instruments, devices or methods for invasive removal or destruction of calculus using mechanical vibrationsSurgical instruments, devices or methods for removing obstructions in blood vessels, not otherwise provided for
A method of preparing a filter for delivery into a body vessel. The filter includes a hub disposed along a longitudinal axis and a plurality of anchor members extending from the hub. Each anchor member includes either a cranial extension or a caudal extension at a distal end thereof. At least one anchor member distal end may be spaced from the hub at each of a first, second, and third distance along the longitudinal axis. The filter also includes a plurality of locator members extending from the hub, the locator members alternatingly interposed between the anchor members.
An apparatus for performing a medical procedure and, in particular, an aortic valvuloplasty, in a vessel for transmitting a flow of fluid. The apparatus comprises a shaft, an inflatable perfusion balloon supported by the shaft and including an internal passage for permitting the fluid flow in the vessel while the perfusion balloon is in an inflated condition, and a valve for controlling the fluid flow within the passage. The valve may be connected to the shaft, or may comprise an elongated tube partially connected to the balloon. The balloon may comprise a plurality of cells in a single cross-section, each cell including a neck, and the valve may be positioned in a space between the shaft and the necks for controlling the fluid flow within the passage. A connector may also be provided to control the position of the valve.
Urinary catheter-insertion kits can include an upper tray fixed to a lower tray and a separator wall positioned over at least a portion of the urinary catheter assembly. The upper tray can include a preformed catheter section configured to accommodate a urinary catheter of a urinary catheter assembly, and a cutout formed through an end portion of the catheter section. A drainage system of the urinary catheter assembly can be disposed in the lower tray, the drainage system including drainage tubing and a drainage receptacle. The drainage tubing can be connected to the urinary catheter through the cutout in the catheter section of the upper tray. Methods of urinary catheterization include use of the urinary catheter-insertion kits.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
(1) Medical devices and apparatus, namely, medical biopsy equipment and instruments, for the diagnosis and treatment of breast cancer and parts and fittings therefor
Medical devices and apparatus, namely, medical biopsy equipment and instruments, for the diagnosis and treatment of breast cancer; and parts and fittings therefor.
92.
ULTRASOUND IMAGING SYSTEM HAVING AUTOMATIC IMAGE PRESENTATION
An ultrasound imaging system includes an interventional medical device having a first tracking element that generates tip location data based on a locator field. An ultrasound probe has an ultrasound transducer mechanism and a second tracking element. The ultrasound transducer mechanism has an active ultrasound transducer array that generates two-dimensional ultrasound slice data at any of a plurality of discrete imaging locations within a three-dimensional imaging volume. The second tracking element generates probe location data based on the locator field. A processor circuit is configured to execute program instructions to generate an ultrasound image for display, and is configured to generate a positioning signal based on the tip location data and the probe location data to dynamically position the active ultrasound transducer array so that the two-dimensional ultrasound slice data includes the distal tip of the interventional medical device.
Breast Biopsy devices for the diagnosis and treatment of breast cancer for use by breast radiologists and breast surgeons, comprising a medical vacuum unit, medical vacuum collection tubes, an ultrasound stylet being a medical instrument, and coaxial cannulae, and parts and fittings therefor, all sold together as a unit, none of the foregoing for cardiac use
Packaging for a medical implant such as a hernia repair prosthetic material includes a carrier and a stiffener. The hernia repair prosthetic material is placed adjacent to the stiffener within the carrier. The carrier assembly is sealed within an outer pouch, such as a foil pouch, and sterilized. When the carrier is being removed from the pouch in preparation for surgery, the stiffener helps prevent the carrier assembly from contacting non-sterile portions of the pouch.
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
B65D 77/04 - Articles or materials enclosed in two or more containers disposed one within another
95.
Apparatus and method for tracking a medical ultrasonic object
A vascular occlusion treatment system includes an ultrasound imaging system having an imaging control circuit communicatively coupled to an ultrasound imaging probe and to a display screen, and an ultrasonic vibration system having an ultrasonic generator operatively coupled to a medical ultrasonic object, such as an ultrasonic catheter. The ultrasonic catheter has a corewire with a distal tip. The ultrasonic generator has a generator control circuit that alternatingly switches between an ultrasonic work frequency and a tracking frequency. The generator control circuit sends a notification to the imaging control circuit when the generator control circuit has switched from the ultrasonic work frequency to the tracking frequency. The imaging control circuit responds by initiating a search in an ultrasound imaging space to locate the distal tip that is vibrating at the tracking frequency, and indicating a location of the distal tip in the ultrasound image displayed on the display screen.
A61B 17/22 - Implements for squeezing-off ulcers or the like on inner organs of the bodyImplements for scraping-out cavities of body organs, e.g. bonesSurgical instruments, devices or methods for invasive removal or destruction of calculus using mechanical vibrationsSurgical instruments, devices or methods for removing obstructions in blood vessels, not otherwise provided for
A61B 17/00 - Surgical instruments, devices or methods
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
09 - Scientific and electric apparatus and instruments
10 - Medical apparatus and instruments
Goods & Services
Computer hardware and software, namely, work station with embedded operating system software for use in performing surgical procedures, none of the foregoing for laboratory use, and parts and fittings therefor. Surgical and medical devices and instruments; medical and surgical lasers; medical generators; laser fibers for medical and surgical purposes; fiber strippers and cleavers, protective glasses, all for use in surgical procedures; urological devices and apparatuses; endourology devices and apparatuses.
97.
Heat Sinks For Catheters, And Systems And Methods Thereof
A catheter assembly including, in some embodiments, a sonic connector at a proximal end of a core wire, a damping mechanism around a proximal end portion of the core wire, and a heat sink connected to the damping mechanism. The sonic connector is configured to couple to an ultrasound-producing mechanism and transmit vibrational energy to the proximal end of the core wire, which core wire includes a distal end portion configured to modify intravascular lesions. The damping mechanism includes a gasket system around the proximal end portion of the core wire in a damping-mechanism bore of the catheter assembly. The damping mechanism is configured to damp the vibrational energy. A system including, in some embodiments, the catheter assembly and the ultrasound-producing mechanism is also disclosed.
A61B 17/22 - Implements for squeezing-off ulcers or the like on inner organs of the bodyImplements for scraping-out cavities of body organs, e.g. bonesSurgical instruments, devices or methods for invasive removal or destruction of calculus using mechanical vibrationsSurgical instruments, devices or methods for removing obstructions in blood vessels, not otherwise provided for
98.
COMPOSITE MEDICAL BALLOON WITH HYBRID OUTER LAYER AND RELATED PRODUCTION METHOD
A composite medical balloon includes a base balloon with first and second tapered portions (108) and a barrel portion (106) therebetween. The base balloon includes one or more fiber layers. A hybrid layer is applied over the base balloon, such as over the fiber layer. The hybrid layer includes a tube (70) for covering the barrel portion (106) and a spiral wrapping (80) for covering one or both of the first and second tapered portions (108). Related methods of forming of such a balloon are also disclosed.
A catheter (10) is provided for relieving compression among blood vessels by introducing a filler into an intravascular space to form a bridge connecting the vessels in order to relieve the compression. The catheter is provided with a shaft (14), expandable elements (16,18) supported by the shaft for reliving compression in the vessel temporarily, and a retractable needle (30) located between the expandable elements. When deployed, such as by using an actuator (40), the needle may deliver the filler to the intervascular space to form a bridge between the vessels for relieving the compression once the catheter is removed.