Disclosed herein are systems and methods for accurately detecting button presses and/or button releases on a keypad of a camera such as an endoscopic camera head. A button press and/or a button release may be detected by determining a change in the sensor voltage output from a magnetic field sensor and identifying a spike in the sensor voltage change. A spike occurs when the slope of the sensor voltage has a magnitude that is greater than a slope threshold, and indicates a button press and/or a button release. Aspects of the disclosure comprise a controller that identifies a spike. The controller may identify a second spike and determine the type of button press based on the duration between the first spike and the second spike. The disclosed systems and methods may further include and apply to a keypad comprising a plurality of buttons, such as closely-spaced buttons and concentric buttons.
G01D 5/12 - Moyens mécaniques pour le transfert de la grandeur de sortie d'un organe sensibleMoyens pour convertir la grandeur de sortie d'un organe sensible en une autre variable, lorsque la forme ou la nature de l'organe sensible n'imposent pas un moyen de conversion déterminéTransducteurs non spécialement adaptés à une variable particulière utilisant des moyens électriques ou magnétiques
A61B 1/00 - Instruments pour procéder à l'examen médical de l'intérieur des cavités ou des conduits du corps par inspection visuelle ou photographique, p. ex. endoscopesDispositions pour l'éclairage dans ces instruments
A urine suction system includes a cannister with a first port, a first tube, and a pump system. The first tube is coupled to the first port and receives fluid from the first port. The pump system includes a pump inlet, a first sensor, a pump, a pump outlet, and a processing circuit. The pump inlet coupled to the first tube and receives the fluid from the first tube. The first sensor provides a signal associated with a pressure of the fluid within the first tube. The pump receives the fluid from the pump inlet. The pump outlet receives the fluid from the pump. The processing circuit includes a memory and one or more processors that receive a signal from the first sensor, determine the pressure based on the signal, and compare the pressure to a pump threshold, cause the pump to provide the fluid at a first rate.
A61M 1/00 - Dispositifs de succion ou de pompage à usage médicalDispositifs pour retirer, traiter ou transporter les liquides du corpsSystèmes de drainage
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
3.
Additive Manufacturing On Machined Assembled Parts
An implant having two adjacent solid parts, a third solid part disposed between the two solid parts, and a porous part extending from the solid parts. The implant is fabricated by a process that includes first assembling the solid parts before additively manufacturing the porous part on surfaces defined by the solid parts. This process may include positioning a first fabricated component adjacent to a second fabricated component such that a side surface of the first fabricated component and a side surface of the second fabricated component form a build surface. Then additively manufacturing a structure on the build surface such that the structure extends across and is permanently fixed to both of the side surfaces of the first and the second fabricated components such that the first and the second fabricated components form part of the implant.
Disclosed are methods and systems that can maintain patient privacy in a video stream of a medical facility by obfuscating all patient identity information such that the patient's identity and medical information is protected. In addition, the system and methods disclosed herein can limit the change in the perspective of the camera based on a defined privacy zone in the medical facility such that the privacy zone is not in the field of view of the camera.
H04N 23/63 - Commande des caméras ou des modules de caméras en utilisant des viseurs électroniques
G06F 21/62 - Protection de l’accès à des données via une plate-forme, p. ex. par clés ou règles de contrôle de l’accès
G06F 21/83 - Protection des dispositifs de saisie, d’affichage de données ou d’interconnexion dispositifs de saisie de données, p. ex. claviers, souris ou commandes desdits claviers ou souris
H04N 5/262 - Circuits de studio, p. ex. pour mélanger, commuter, changer le caractère de l'image, pour d'autres effets spéciaux
H04N 5/272 - Moyens pour insérer une image de premier plan dans une image d'arrière plan, c.-à-d. incrustation, effet inverse
H04N 23/661 - Transmission des signaux de commande de la caméra par le biais de réseaux, p. ex. la commande via Internet
5.
METHOD AND APPARATUS FOR PASSING SUTURE THROUGH TISSUE
Described are suture passers including a hollow tube having a distal end, a proximal end, and a lumen extending to the distal end; and a suture manipulator slidably disposed in the lumen of the hollow tube and having a distal end that is extendable from and retractable into a distal portion of the hollow tube. The distal portion of the suture manipulator includes a catching surface for catching suture and pulling the suture into the lumen so that a loop of the suture is located in the lumen. The width of a gap between an inner surface of the distal portion of the hollow tube and a side surface of the distal portion of the suture manipulator is less than the width of the distal portion of the suture manipulator, so that the suture is compressed in the gap when the suture is pulled into the lumen.
A61B 17/04 - Instruments, dispositifs ou procédés chirurgicaux pour refermer les plaies ou les maintenir ferméesAccessoires utilisés en liaison avec ces opérations pour la suture des plaiesSupports ou emballages pour aiguilles ou matériaux de suture
A61B 17/00 - Instruments, dispositifs ou procédés chirurgicaux
A61B 17/06 - AiguillesSupports ou empaquetages pour aiguilles ou matériaux de suture
Disclosed herein are viewing systems configured for viewing an image of a biological object illuminated with light and a viewing device (e.g., loupes, glasses, etc.) and methods for operation thereof. The viewing device comprises a plurality of viewing modes: a white light mode, a fluorescent light mode, and an overlay mode, and a shutter that opens and closes in accordance with the viewing mode. An overlay image is an image of the biological object when the biological object is illuminated with both white light and fluorescent light, causing the overlay image to be an overlay of the white light image and the fluorescent light image. The disclosed systems and methods allow a user (e.g., a surgeon, medical staff, etc.) to preserve the ergonomics offered by eyewear while providing fluorescent viewing capabilities, particularly with visible fluorescent dyes.
H04N 23/56 - Caméras ou modules de caméras comprenant des capteurs d'images électroniquesLeur commande munis de moyens d'éclairage
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
G02F 1/133 - Dispositions relatives à la structureExcitation de cellules à cristaux liquidesDispositions relatives aux circuits
G02F 1/137 - Dispositifs ou dispositions pour la commande de l'intensité, de la couleur, de la phase, de la polarisation ou de la direction de la lumière arrivant d'une source lumineuse indépendante, p. ex. commutation, ouverture de porte ou modulationOptique non linéaire pour la commande de l'intensité, de la phase, de la polarisation ou de la couleur basés sur des cristaux liquides, p. ex. cellules d'affichage individuelles à cristaux liquides caractérisés par l'effet électro-optique ou magnéto-optique, p. ex. transition de phase induite par un champ, effet d'orientation, interaction entre milieu récepteur et matière additive ou diffusion dynamique
G03B 7/08 - Réglage effectué uniquement sur la base de la réponse, à l'intensité de l'éclairage reçu par l'appareil, d'un dispositif incorporé sensible à la lumière
A light cable for conveying light from a light source to an endoscope includes a first connector at a proximal end of the light cable for connecting to the light source; a second connector at a distal end of the light cable for connecting to the endoscope; a light guide for conveying light received from the light source to the endoscope; a first wireless antenna positioned at the proximal end for wireless communication with the light source; a second wireless antenna positioned at the distal end for wireless communication with the endoscope; and a passive repeater connecting the first wireless antenna and the second wireless antenna for conveying signals between the first and second wireless antennas.
A61B 1/07 - Instruments pour procéder à l'examen médical de l'intérieur des cavités ou des conduits du corps par inspection visuelle ou photographique, p. ex. endoscopesDispositions pour l'éclairage dans ces instruments avec dispositifs d'éclairement utilisant des moyens conduisant la lumière, p. ex. des fibres optiques
A61B 1/00 - Instruments pour procéder à l'examen médical de l'intérieur des cavités ou des conduits du corps par inspection visuelle ou photographique, p. ex. endoscopesDispositions pour l'éclairage dans ces instruments
A61B 1/06 - Instruments pour procéder à l'examen médical de l'intérieur des cavités ou des conduits du corps par inspection visuelle ou photographique, p. ex. endoscopesDispositions pour l'éclairage dans ces instruments avec dispositifs d'éclairement
A method includes operating a motor of a handheld device when the handheld device is connected to a mechanical arm and operating the motor of the handheld device when the handheld device is disconnected from the mechanical arm.
A61B 17/00 - Instruments, dispositifs ou procédés chirurgicaux
A61B 17/16 - Instruments pour réaliser une ostéoclasieForets ou ciseaux pour osTrépans
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
9.
Filter Assembly For Filtering Smoke Evacuated With A Medical Waste Collection System Including A Vacuum
Systems and methods for evacuation of surgical smoke. A capital component may include a vacuum source, and a controller. A filter assembly is configured to be removably coupled to the capital component and include a housing defining a socket for connecting a smoke evacuation tube, and include a flap for selectively covering the socket. The sensor is configured to detect the position of the flap relative to the socket. The controller may be configured to operate the system based on the position of the flap relative to the socket, as detected by the sensor. The controller may be configured to enable disable, or adjust the operation of the vacuum source based on the signal, and/or open or close a valve associated with the vacuum source. Assemblies and methods for removing filter media from the housing of the filter assembly are also disclosed.
A61M 1/00 - Dispositifs de succion ou de pompage à usage médicalDispositifs pour retirer, traiter ou transporter les liquides du corpsSystèmes de drainage
A61B 18/00 - Instruments, dispositifs ou procédés chirurgicaux pour transférer des formes non mécaniques d'énergie vers le corps ou à partir de celui-ci
10.
UTILIZING THE PRESSURE-VOLUME RELATIONSHIP TO IDENTIFY LUNG CONDITION
Systems, devices, and methods for determining a treatment decision for a subject during assisted ventilation are described herein. In an example method, a pressure and a volume of air in an airway of the subject is determined during one or more ventilation cycles. An airway parameter of the subject is determined based on generating and analyzing a pressure-volume relationship of the subject. A treatment decision is identified based on analyzing the airway parameter. In various implementations, a respiratory condition of the subject is determined based on analyzing the airway parameter of the subject. The example method can be implemented into a monitor-defibrillator or another portable medical device. Together, the methods can improve the treatment of subjects receiving CPR who have respiratory conditions.
A61B 5/091 - Mesure du volume des gaz inspirés ou expirés, p. ex. pour déterminer la capacité pulmonaire
A61B 5/085 - Mesure de l'impédance des organes respiratoires ou de l'élasticité pulmonaire
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/093 - Mesure du volume des gaz inspirés ou expirés, p. ex. pour déterminer la capacité pulmonaire en expirant dans, ou en inspirant à partir d'une enceinte expansible, p. ex. un soufflet ou un sac expansible
A patient care delivery system including a first kit including a first tool, and a dock assembly including a base, an arm coupled to the base and extending from the base, a first sensor disposed within the base or the arm, an indicator positioned on the base or the arm, and a processing circuit disposed within the base or the arm. The processing circuit includes a memory and one or more processors. The one or more processors are configured to receive a first signal from the first sensor when the first kit is at least one of coupled to the arm, suspended in front of the arm, or adjacent to the arm, after receiving the first signal, cause the indicator to provide a first indication to a user, and after not receiving the first signal, cause the indicator to provide a second indication to the user.
A46B 11/06 - Brosses à réservoir ou autre système permettant l'application de produits, p. ex. peintures, pâtes, eau reliées à un tuyau d'alimentation
A46B 15/00 - Autres brossesBrosses avec aménagements additionnels
A61B 17/00 - Instruments, dispositifs ou procédés chirurgicaux
A61G 12/00 - Équipements pour donner des soins, p. ex. dans les hôpitaux, non couverts par l'un des groupes , p. ex. chariots pour le transport des médicaments ou de la nourritureTableaux d'ordonnances
G16H 40/00 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux
Systems, devices, and methods are described herein for adjusting the spot size of light provided from a surgical light by translating a focus panel relative to a plurality of light emitters. The focus panel can be mounted to the housing of the surgical light such that the focus panel can translate relative to the housing in an axial direction toward and away from the plurality of light emitters. The focus panel can engage with one or more tracks that are movably mounted relative to the housing and controlled via at least one actuator. The actuator(s) can be configured to translate the focus panel towards or away from the plurality of light emitters to adjust the spot size of light provided by the surgical light via the engagement between the focus panel and the one or more tracks.
F21V 17/02 - Fixation des parties constitutives des dispositifs d'éclairage, p. ex. des abat-jour, des globes, des réfracteurs, des réflecteurs, des filtres, des écrans, des grilles ou des cages de protection avec possibilité de réglage
A patient support apparatus is provided including a deck for supporting a mattress thereon and a barrier mounted relative to the deck. The barrier has a barrier body, with opposed first and second outer sides, a barrier outer perimeter, and a through opening extending there through from the first outer side to the second outer side. The patient support apparatus may include a cover for covering the through opening and which is mounted at the barrier body.
An electrode probe for radiofrequency ablation. A shaft extends from a hub and defines at least one lumen. A lead is disposed within the lumen, and at least one emitter is coupled to the lead. The emitter(s) are coupled onto a flexible distal portion of the shaft, such as through a swaging operation. The emitter(s) include a slotted portion defining slots sized for the conductive material to be deformed with swaging of the emitter onto the flexible distal portion. The emitter(s) may include a slotted portion and end portions, and the lead may be secured to one of the end portions through a laser welding operation. The slots may have a slot pitch within a range of 0.150 to 0.400 millimeters. The slots may be circumferentially disposed with a cut angle within a range of 50 to 90 degrees. Methods of manufacturing the electrode probe are also disclosed.
A61B 18/00 - Instruments, dispositifs ou procédés chirurgicaux pour transférer des formes non mécaniques d'énergie vers le corps ou à partir de celui-ci
A hemostatic valve for sealing a medical device includes a unibody elongate member having a first end, a second end, and a central lumen extending therebetween, wherein the unibody elongate member is pliable. The hemostatic valve includes a reinforcement structure extending along at least a portion of the unibody elongate member, wherein the reinforcement structure is coupled to the unibody elongate member. An active tensioning mechanism including an actuator coupled to the unibody elongate member, wherein the actuator is moveable between (a) a first position wherein the central lumen is constricted and sealed, and (b) a second position wherein the central lumen is open, and wherein the tensioning mechanism includes at least one filament extending at least partially around the unibody elongate member. The hemostatic valve includes a biasing member configured to bias the actuator to the first position.
A61M 39/06 - Soupapes hémostatiques, c.-à-d. éléments formant joint autour d'une aiguille, d'un cathéter ou similaire, et se fermant après leur retrait
18.
Interactive Techniques For Activation Of A Surgical System
Surgical systems and methods involve a surgical robot configured to support and move a surgical tool, a tracking system configured to track a position of a surgical staff member, and one or more controllers coupled to the surgical robot and the tracking system. The controller(s) define a first virtual zone and a second virtual zone relative to the surgical robot, detect a positioning of the surgical staff member in the first virtual zone based on tracked position data, and in response, trigger a first control mode for the surgical robot. The controller(s) further detect a positioning of the surgical staff member in the second virtual zone and, in response, trigger a second control mode for the surgical robot that is different from the first control mode.
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A method of visualizing an implant plan includes visualizing, on a graphical user interface, a bone and an implant in a planned pose relative to the bone, providing, on the graphical user interface, a marking at a portion of the implant associated with violation of a criterion by the planned pose, and removing the marking from the graphical user interface in response to an update to the planned pose that resolves the violation of the criterion.
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 17/02 - Instruments, dispositifs ou procédés chirurgicaux pour maintenir les blessures ouvertes, p. ex. rétracteursÉcarteurs
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/35 - Robots chirurgicaux pour la téléchirurgie
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
A61F 2/46 - Outils particuliers pour l'implantation des articulations artificielles
A hemostatic valve for sealing a medical device includes a unibody elongate member having a first end, a second end, and a central lumen extending therebetween, wherein the unibody elongate member is pliable. The hemostatic valve includes a reinforcement structure extending along at least a portion of the unibody elongate member, wherein the reinforcement structure is coupled to the unibody elongate member. An active tensioning mechanism including an actuator coupled to the unibody elongate member, wherein the actuator is moveable between (a) a first position wherein the central lumen is constricted and sealed, and (b) a second position wherein the central lumen is open, and wherein the tensioning mechanism includes at least one filament extending at least partially around the unibody elongate member. The hemostatic valve includes a biasing member configured to bias the actuator to the first position.
A61M 39/06 - Soupapes hémostatiques, c.-à-d. éléments formant joint autour d'une aiguille, d'un cathéter ou similaire, et se fermant après leur retrait
An example method includes generating, by a first device, an instruction or an alert; outputting, by the first device, a first output signal indicating the instruction or the alert; transmitting, by the first device to a second device, a communication signal indicating the instruction or the alert; and outputting, by the second device, a second output signal indicating the instruction or the alert. The second output signal has a common characteristic with the first output signal.
A computing system includes a mixed reality (MR) visualization device and one or more processors implemented in circuitry may be configured to prompt a user wearing a visualization device to direct their gaze toward a physical registration region of a physical object that corresponds to a virtual registration region of a virtual model of the physical object; provide the user, via a user interface of the visualization device, a visual cue in a vicinity of the physical registration region; perform a registration operation to register the physical registration region with the virtual registration region; and while performing the registration operation, change the visual cue over time to indicate to the user a progress toward registration of the physical registration region with the virtual registration region.
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
G06F 3/01 - Dispositions d'entrée ou dispositions d'entrée et de sortie combinées pour l'interaction entre l'utilisateur et le calculateur
23.
Robotic Surgical Systems And Methods For Guiding A Tool Along A Path Using Hybrid Automated/Manual Control
Surgical systems and methods involve a manipulator supporting a tool and a force/torque sensor to measure forces/torques applied to the tool by a user. A control system obtains a predetermined tool path for the tool and commands the manipulator to perform automated advancement of the tool along the predetermined tool path in a first path direction according to a predetermined feed rate. During the automated advancement, the control system receives input from the force/torque sensor in response to forces/torques applied by the user, determines a virtual acceleration vector based on the input, and evaluates an effect of the virtual acceleration vector on the automated advancement. Based on the evaluation, the control system determines an effective feed rate and effective path direction relative to the predetermined tool path and determines a commanded action for the manipulator and the tool based on the effective feed rate and effective path direction.
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 34/32 - Robots chirurgicaux opérant de façon autonome
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
A cannula for penetrating bone includes a hub and a shaft extending from the hub along a longitudinal axis. The shaft includes an outer circumferential surface, and an inner circumferential surface defining a lumen. At the distal end of the shaft is a cutting tip with cutting teeth arranged annularly to penetrate bone when rotated about the longitudinal axis. Each cutting tooth has a leading cutting surface facing the direction of rotation, a distal edge, a proximal edge, and a proximally sloping relief surface. The leading cutting surface may be chamfered from one circumferential surface to the other, forming a leading cutting edge. The relief surface may be sloped proximally from one circumferential surface to the other, forming a shear cutting edge. The leading cutting surface or the leading edge may be oriented at an angle of attack, which may be open to rotation.
Detecting and analyzing chest compressions via airway parameters, and performing one or more actions based on the compression analysis is described. In some examples, a sensor detects a carbon dioxide (CO2) parameter associated with a subject, and a processor generate CO2 data indicating the CO2 parameter. The processor further identifies a chest compression artifact exhibited in the CO2 data, determines, based on the chest compression artifact, a chest compression parameter associated with chest compressions that are being administered to the subject, and causes performance of an action based on an analysis of the chest compression parameter.
A patient support apparatus having a control system is provided that manages the delivery of electrical power to a CPR valve manifold actuator that opens or closes the CPR valve manifold. The control system may manage the power delivery process both when the patient support apparatus is operating on a bed-based DC power supply, such as a bed-based battery power supply, and/or when the patient support apparatus is plugged into an external source of electrical power, such as a conventional Alternating Current (AC) power outlet.
A61G 7/015 - Lits spécialement conçus pour donner des soinsDispositifs pour soulever les malades ou les personnes handicapées comportant un cadre de sommier réglable divisé en plusieurs parties réglables, p. ex. pour la position dite "Gatch"
A61G 7/018 - Mécanismes de commande ou d'entraînement
A61H 31/00 - Respiration artificielle par une force appliquée sur la poitrineStimulation du cœur, p. ex. massage cardiaque
30.
Patient Transport Apparatus Having Adaptive Stair Braking
Systems and methods for operating a patient transport apparatus including a motor and controller in communication with the motor. The controller is configured to determine an average duty cycle of a pulse-width modulation signal during steady state operation of the motor in a drive mode, the average duty cycle of the pulse-width modulation signal corresponding to a load acting on the patient transport apparatus, activate a ramp-down phase of the motor in response to the controller detecting at least one of an absence of user engagement with a activation input control and a fault condition, and adjust the speed of the motor during the ramp¬down phase based on the average duty cycle of the pulse-width modulation signal corresponding to load acting on the patient transport apparatus for smoothing a transition in operation from the drive mode to a brake mode.
A61G 5/06 - Fauteuils ou moyens de transport personnels spécialement adaptés pour des personnes handicapées, p. ex. fauteuils roulants avec dispositions pour franchir les obstacles, p. ex. pour monter les escaliers
A61G 5/08 - Fauteuils ou moyens de transport personnels spécialement adaptés pour des personnes handicapées, p. ex. fauteuils roulants pliables
A61G 5/10 - Parties constitutives, détails ou accessoires
31.
SYSTEMS AND METHODS FOR CAPTURING, DISPLAYING, AND MANIPULATING MEDICAL IMAGES AND VIDEOS
A video analysis system comprises an image capture device and a display assembly configured to display one or more images captured by the image capture device. The system captures a first series of video frames in a first spectrum and a second series of video frames in a second spectrum, wherein the second series of video frames is captured simultaneously with capturing of the first series of video frames. The system identifies a first feature in one or more frames of the first series of video frames and applies a tracking algorithm to track the first feature in the first series of video frames. The system identifies a region in one or more frames of the second series of video frames based on the tracking algorithm applied to the first series of video frames.
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
A glenosphere handling tool, which can be an impactor, is provided that includes an elongate body and a retention portion. The retention portion is disposed at a distal end of the elongate body. The retention portion includes a plurality of wall segments of the elongate body separated from each other by one or more slots. The slot(s) extends proximally from the distal end of the elongate body. The retention portion also includes an enlarged periphery at the distal end of the elongate body. The enlarged periphery comprising a proximally facing edge configured to engage an inner wall surface of a glenosphere. The retention portion is configured such that when the retention portion is in a free state the proximally facing edge faces and may contact a surface of a glenosphere to retain the glenosphere. The retention portion is configured to be deflected at the distal end of the elongate body such that the enlarged periphery has a reduced profile for separating the handling tool from a glenosphere.
A connector for detachably coupling an implant to a delivery wire, includes: a structure having a distal portion coupled to a proximal end of the implant, and a proximal portion coupled to a distal end of the delivery wire; wherein the structure comprises a first element formed by a first material, and second elements formed by a second material, wherein the second elements are distributed in the first element.
A61B 17/12 - Instruments, dispositifs ou procédés chirurgicaux pour ligaturer ou comprimer par un autre moyen les parties tubulaires du corps, p. ex. les vaisseaux sanguins ou le cordon ombilical
A61F 2/95 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes
34.
SYSTEM AND METHOD FOR INSERTING A SURGICAL IMPLANT
An electric power tool for inserting a surgical implant includes a housing, an electric motor, and a controller configured to receive a motor-parameter signal containing multiple frequency components during implant insertion. The controller processes portions of the signal using frequency-selective techniques, including low-pass and high-pass filtering, short-time Fourier transforms, and Hilbert transforms, to generate a signal feature corresponding to magnitude, power, or energy of selected frequency content over time. Based on first and second characteristics of the feature, the controller detects driving events and determines dynamic thresholds used to regulate operation of the motor, including issuing stop, limit, or activation commands. Additional embodiments include multi-order filters, phase and variability metrics, screw-type classification derived from threshold signals, and algorithms adapted for multiple insertion states such as inrush, breach, and drive.
An absorbent medical sheet assembly includes an impermeable layer and a permeable layer coupled to the impermeable layer. The permeable layer is in confronting relation to the impermeable layer and cooperating with the impermeable layer to define a cavity therebetween. The absorbent medical sheet includes an absorbent dam positioned between the impermeable layer and the permeable layer such that the cavity extends around an entirety of the absorbent dam.
A61F 13/15 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons
There is described a medical device (100), comprising:—an airway adaptor (212, 312) configured to be connected to an airway of a patient;—a first sensor (104, 202, 302) a configured to detect a first parameter of a space fluidly connected to the airway adaptor, the first parameter being for example an air flow rate, an air pressure, an O2 level, a CO2 level, or a humidity level;—a second sensor (104, 204, 304) configured to detect a second parameter of the space, the second parameter being for example an O2 level or an air pressure;—a display (216, 316); and-a processor (510) configured to determine a relationship between the first parameter and the second parameter, based on determining that the relationship has changed over multiple ventilations, identify a leak between the airway adaptor and the airway of the patient, generate an alert indicating the leak, and cause the display to output the alert. The medical device may comprise for example a bag-valve-mask (BVM) and the airway adaptor may comprise for example a mask, a supraglottic device, or an endotracheal tube.
Systems, devices, and methods for determining a treatment decision for a subject during cardiopulmonary resuscitation (CPR) are described herein. In an example method, a physiological parameter is detected during a first time period when treatment is administered to the subject and during a second time period when treatment is paused. The physiological parameter detected during treatment and the physiological parameter detected outside of treatment are analyzed. A treatment decision is identified based on analyzing the physiological parameter during treatment and outside of treatment. The example method can be implemented into a monitor-defibrillator or another portable medical device. Together, the methods can improve the treatment of subjects receiving CPR by reducing unnecessary treatment.
A joint simulator for simulating biomechanical properties of a joint includes a first end simulating a first bone of the joint, a second end simulating a second bone of the joint, at least one flexible band simulating a ligament of the joint, a first surface component connected to the first end, and a second surface component connected to the second end. The flexible band couples the first and second ends and is adjustable to simulate stresses corresponding to the first and second ends. The first surface component simulates a distal end of the first bone and the second surface component simulates a proximal end of the second bone.
An absorbent medical sheet assembly includes an impermeable layer and a permeable layer coupled to the impermeable layer. The permeable layer is in confronting relation to the impermeable layer and cooperating with the impermeable layer to define a cavity therebetween. The absorbent medical sheet includes an absorbent dam positioned between the impermeable layer and the permeable layer such that the cavity extends around an entirety of the absorbent dam.
A61F 13/84 - Accessoires, non prévus ailleurs, pour garnitures absorbantes
A61F 13/15 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons
A61F 13/511 - Feuille supérieure, c.-à-d. revêtement ou couche perméable dirigée vers la peau
A61F 13/514 - Feuille inférieure, c.-à-d. revêtement ou couche imperméable la plus éloignée de la peau
Techniques for electronic devices including medical devices and non-medical devices are described. An example method includes moving from a dynamic real-time snapshot of an ECG to a historical snapshot of the ECG; and generating the dynamic real-time snapshot of the ECG and the historical snapshot of the ECG, the historical snapshot of the ECG being selected from among a dynamic historical snapshot of the ECG or a static historical snapshot of the ECG. The dynamic real-time snapshot includes an ECG presented in an electronic format. The historical snapshot includes an ECG presented in a pseudo-paper format.
Disclosed herein are automatic-locking and automatic-unlocking syringes, and associated systems and methods. In some embodiments, a syringe can include a barrel, a plunger assembly slidably positioned within the barrel, and a locking assembly coupled to the barrel. The syringe is configured to (i) automatically lock the plunger assembly to the locking assembly when the plunger assembly is withdrawn through the barrel with a vacuum in the barrel, (ii) automatically unlock the plunger assembly from the locking assembly when the barrel no longer experiences vacuum and/or experiences negligible vacuum, and/or (iii) inhibit or even prevent automatic locking of the plunger assembly to the locking assembly when the plunger assembly is withdrawn through the barrel with no and/or negligible vacuum within the barrel.
A61M 5/315 - PistonsTiges de pistonGuidage, blocage, ou limitation des mouvements de la tigeAccessoires disposés sur la tige pour faciliter le dosage
A61M 5/20 - Seringues automatiques, p. ex. avec tige de piston actionnée automatiquement, avec injection automatique de l'aiguille, à remplissage automatique
46.
COMPUTER-IMPLEMENTED SURGICAL PLANNING BASED ON BONE LOSS DURING ORTHOPEDIC REVISION SURGERY
A surgical assistance system may obtain a pre-revision model of a bone of a patient. The prerevision model of the bone represents a pre-revision state of the bone after a prior orthopedic surgery on the bone. In this example, an orthopedic prosthesis was attached to the bone during the prior orthopedic surgery. Additionally, the surgical assistance system may obtain intra-revision imaging data of the bone. The intra-revision imaging data represents an intra-revision state of the bone during the orthopedic revision surgery after removal of the orthopedic prosthesis from the bone. The surgical assistance system may determine, based on the intra revision imaging data, damaged and intact parts of the bone. The surgical assistance system may then generate a second intra-revision model of the bone by modifying the pre-revision model of the bone to exclude damaged parts of the bone.
A61F 2/46 - Outils particuliers pour l'implantation des articulations artificielles
A61B 17/16 - Instruments pour réaliser une ostéoclasieForets ou ciseaux pour osTrépans
A61B 17/17 - Dispositifs de guidage pour les forets
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
A61B 90/50 - Supports pour instruments chirurgicaux, p. ex. bras articulés
Surgical or medical systems and methods involve a manipulator to facilitate collaborative interaction with a human. A control system is coupled to the manipulator and is configured to acquire robotic data from the manipulator during the collaborative interaction. The control system implements a machine learning model that is configured to receive and process the robotic data to determine an interaction style of the human in collaborating with the manipulator. The control system customizes a physical feel of the manipulator based on the interaction style.
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
48.
Machine Learning Assisted Surgical Decision Systems And Methods
Disclosed herein is a system for machine learning assisted surgical planning. The system can include a data acquisition module configured to collect preoperative data, intraoperative data, and postoperative data. The preoperative data can include any of imaging data, patient-reported outcome measures and functional metrics. The intraoperative data can include kinematic assessment of a knee joint. The postoperative data can include any of functional recovery metrics, radiographic data, and adverse event tracking. The system can include a machine learning model configured to process the preoperative data, intraoperative data, and postoperative data to identify patterns and relationships between surgical planning attributes and patient-specific outcomes, and generate predictive outputs including recommendations for the surgical planning attributes.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p. ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A wedge cushioning system for supporting a lower limb of a patient includes a wedge assembly. The wedge assembly includes a wedge pad configured to cushion the lower limb of the patient, a first wedge wing pivotably coupled to a first side of the wedge pad and selectively pivotable between a first lowered position and a first raised position, a second wedge wing pivotably coupled to a second side of the wedge pad and selectively pivotably between a second lowered position and a second raised position independent of the first wedge wing, and a strap configured to be releasably coupled between the first wedge wing and the second wedge wing. The second side of the wedge pad is opposite the first side of the wedge pad.
An example method includes detecting, by a sensor among an array of sensors in a chest-mounted apparatus, a compression applied to a chest of a subject by a compressor. By analyzing a position of the sensor among the array of sensors, a position of the compression is determined along a plane that is normal to an anterior-posterior direction. The example method further includes determining that the position of the compression is outside of a predetermined target range; and in response to determining that the position of the compression is outside of the predetermined target range, outputting an instruction to reposition the compressor.
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
An example method performed by a computing device includes receiving patient data indicating physiological parameters of a subject during a rescue event; generating simulated patient data by altering the patient data; and generating a simulated medical device user interface (UI) indicating the simulated patient data. The example method further includes receiving an input signal from a user and displaying the simulated medical device UI by displaying a first segment of the simulated patient data indicating a medical condition that is responsive to a treatment; and displaying a recommendation to administer the treatment. In response to displaying the recommendation to administer the treatment and in response receiving the input signal, the example method includes displaying a second segment of the simulated patient data indicating a simulated response to the treatment.
A person support apparatus includes a first transceiver adapted to wirelessly communicate with a second transceiver of a headwall interface that is positioned off of the person support apparatus. A communication link is automatically established between the first and second transceivers without requiring a user of the person support apparatus to activate a designated control and without requiring the user to identify the headwall interface. The first transceiver includes a unique identifier assigned to the headwall interface in its messages to the headwall interface. The first transceiver may also automatically transmit a disconnect signal to the headwall interface indicating the termination of the communication link is not accidental. The disconnect signal is sent based on one or more of the following: (1) a brake being off, (2) an A/C power cord being unplugged; and/or (3) a signal strength between the transceivers decreasing.
Surgical systems and method for manipulation of a bone involve a surgical manipulator having a robotic arm configured to support and move a surgical instrument that includes an energy applicator, and a sensor configured to sense forces/torques applied to one or both of the surgical instrument and the energy applicator. Controller(s) are coupled to the manipulator and the sensor. In a semi-autonomous mode, the controller(s) operate the manipulator to move the energy applicator along a predefined tool path according to a feed rate, utilize the sensor to sense forces/torques applied to the energy applicator by the bone, and adjust the feed rate based on the sensed forces and torques. In a manual mode, the controller(s) utilize the sensor to sense forces and torques applied to the surgical instrument by a user and move the energy applicator based on the sensed forces and torques to manipulate the bone.
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 17/16 - Instruments pour réaliser une ostéoclasieForets ou ciseaux pour osTrépans
A61B 18/00 - Instruments, dispositifs ou procédés chirurgicaux pour transférer des formes non mécaniques d'énergie vers le corps ou à partir de celui-ci
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
B25J 13/08 - Commandes pour manipulateurs au moyens de dispositifs sensibles, p. ex. à la vue ou au toucher
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
54.
METHODS OF TREATING DELAYED UNION AND NONUNION FRACTURES USING PLATELET-DERIVED GROWTH FACTOR COMPOSITIONS
The present disclosure provides methods for treating delayed union or nonunion fractures in a bone More specifically, the present disclosure provides methods of inducing bone formation in a delayed union or nonunion fracture in a bone comprising: applying to a site of delayed union or nonunion fracture a composition comprising a platelet-derived growth factor (PDGF) solution disposed in a biocompatible matrix.
A61L 27/42 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice inorganique
A61L 27/54 - Matériaux biologiquement actifs, p. ex. substances thérapeutiques
C04B 35/447 - Produits céramiques mis en forme, caractérisés par leur compositionCompositions céramiquesTraitement de poudres de composés inorganiques préalablement à la fabrication de produits céramiques à base d'oxydes à base de phosphates
55.
Wedge for a patient turning and positioning system
Described are systems and methods for visualizing planned bone removal. A two-dimensional image of at least a portion of a joint is received. An alignment of a pre-generated three-dimensional model of the at least a portion of the joint with the two-dimensional image is determined based on one or more features in the two-dimensional image that are associated with the at least a portion of the joint. The pre-generated three-dimensional model includes a representation of planned bone removal. An overlay image is generated based on the determined alignment. The overlay image includes an overlay of at least a portion of the representation of planned bone removal on the two-dimensional image. A visualization including the overlay image is then displayed.
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
57.
Robotic Surgical System With Density-Based Trajectory Planning And Guidance
A robotic surgery system prepares a bone to receive an implant having screw openings. The system includes a robotic manipulator, interchangeable cutting tools, and a controller. The controller obtains a surgical plan defining a resection plane, implant location, and screw‑opening locations, and operates the manipulator to create a resected surface. A bone mineral density (BMD) distribution comprising voxels with associated density values is obtained, and a subset of voxels below the resected surface is identified. The controller groups selected voxels into candidate voxel clusters, computes a collective density metric for each cluster, and selects, for each screw opening, a candidate voxel cluster having a greater metric than other clusters. Based on each selected cluster, the controller determines a screw trajectory that passes through the cluster, associates a virtual line haptic object with each trajectory, and guides the second cutting tool along the haptic objects to form pilot holes.
A61F 2/46 - Outils particuliers pour l'implantation des articulations artificielles
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 17/16 - Instruments pour réaliser une ostéoclasieForets ou ciseaux pour osTrépans
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
58.
ROBOTIC SURGERY SYSTEM WITH CUSTOM HAPTIC APPROACH REGION
A method includes determining a contour of a bone model at a cross-section intersected by a haptic object corresponding to a planned resection, the haptic object including a resection region intersecting the bone model and an approach region extending away from the resection region. The method also includes morphing the approach region of the haptic object based on the contour of the bone model. The method also includes controlling a surgical robot using the approach region using the morphed haptic object.
An example method includes: receiving images of a vessel having an aneurysm captured by an image-capture device; reconstructing using the images, the vessel to generate a model of the vessel; determining taking foreshortening effect into consideration, a final length of a stent when the stent is deployed inside the model of the vessel to divert flow from the aneury sm; visually presenting a display of the stent deployed within the model of the vessel; and providing parameters of the stent including apposition and pore density of the stent.
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 6/50 - Appareils ou dispositifs pour le diagnostic par radiationsAppareils ou dispositifs pour le diagnostic par radiations combinés avec un équipement de thérapie par radiations spécialement adaptés à des parties du corps spécifiquesAppareils ou dispositifs pour le diagnostic par radiationsAppareils ou dispositifs pour le diagnostic par radiations combinés avec un équipement de thérapie par radiations spécialement adaptés à des applications cliniques spécifiques
A61F 2/82 - Dispositifs maintenant le passage ou évitant l’affaissement de structures tubulaires du corps, p. ex. stents
A61F 2/90 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles
G16H 50/50 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour la simulation ou la modélisation des troubles médicaux
61.
METHODS AND SYSTEMS FOR CHARACTERIZING TISSUE OF A SUBJECT
The present disclosure relates generally to medical imaging, and more specifically to machine-learning techniques for analyzing and generating medical images (e.g., to aid diagnosis and/or treatment of diseases). An exemplary method of displaying a predicted future state of a tissue of a subject includes receiving a fluorescence image of the tissue of the subject, providing the fluorescence image to a generator of a trained generative adversarial (“GAN”) model, obtaining, from the generator, a simulated white-light image depicting the predicted future state of the tissue of the subject, and displaying, on the display, the simulated white-light image depicting the predicted future state of the tissue of the subject.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
62.
METHOD AND SYSTEM FOR MAXIMIZING THE OUTPUT OF SURGICAL LIGHTS
A surgical light is provided including a housing, at least one light source within the housing and emitting light from the housing that substantially converges on a focal area, and at least two locating light sources emitting visual locating light along lines, the lines of visual locating light substantially uniting at a focal area. Methods of locating light using the surgical light include illuminating an object with the light emitting from the plurality of light sources, illuminating the object with the visual locating light along the lines emitted from the at least two locating light sources, and adjusting a position of the surgical light to form a point at an area of interest on the object with the lines of visual locating light.
H05B 47/115 - Commande de la source lumineuse en réponse à des paramètres détectés en détectant la présence ou le mouvement d'objets ou d'êtres vivants
F21V 23/04 - Agencement des éléments du circuit électrique dans ou sur les dispositifs d’éclairage les éléments étant des interrupteurs
F21W 131/205 - Éclairage pour un usage médical pour les salles d'opération
G01S 15/88 - Systèmes sonar, spécialement adaptés à des applications spécifiques
H05B 45/10 - Commande de l'intensité de la lumière
H05B 47/16 - Commande de la source lumineuse par des moyens de minutage
An ambulance cot loading and unloading system for an emergency vehicle includes a base for mounting in the emergency vehicle and an arm mounted for linear movement along the base, wherein the arm configured to support a cot while the cot is being loaded into or unloaded from the emergency vehicle. The ambulance cot loading and unloading system further includes an indicator mounted relative to the arm and a control system, which is in communication with the indicator and configured to generate a status indication of the cot loading and unloading system at the indicator.
A61G 3/02 - Chargement ou déchargement des moyens de transport personnelsMoyens pour faciliter l'accès des personnes handicapées aux véhicules ou leur sortie des véhicules
A61G 1/06 - Supports pour brancards, p. ex. pour être placés dans ou sur des véhicules
A61G 3/08 - Logement ou immobilisation des chaises roulantes
B65G 35/06 - Transporteurs mécaniques non prévus ailleurs comportant un porte-charges se déplaçant le long d'un circuit, p. ex. d'un circuit fermé, et adapté pour venir en prise avec l'un quelconque des éléments de traction espacés le long du circuit
A modular patient support system includes a base assembly and a litter assembly. The litter assembly may include one of a first litter assembly including a first litter support structure having a first configuration and a second litter assembly including a second litter support structure having a second configuration, different than the first configuration.
A61G 7/012 - Lits spécialement conçus pour donner des soinsDispositifs pour soulever les malades ou les personnes handicapées comportant un cadre de sommier réglable pour élever ou abaisser tout le cadre du sommier
A61G 7/05 - Parties constitutives, détails ou accessoires de lits
69.
Medical Waste Collection System For Collecting Medical Waste During A Medical Procedure
A medical waste collection system for collecting waste material. A level sensor is coupled to at least one waste container to generate a signal indicating a fluid level of waste material therein. A controller is configured to operate a light source assembly based on the signal such that a portion of the interior of the waste container disposed beneath the fluid level of the waste material is illuminated. A cover assembly may include a rack and pinion and/or polarizing segments to selectively limit visibility of portions of the waste container. The controller may initiate an unclogging protocol to create a pressure differential between an upper waste container and a lower waste container based on a determination that a transfer valve between the waste containers may be clogged. The determination may be based on a rate of change of the fluid level as measured by the level sensor(s).
A61M 1/00 - Dispositifs de succion ou de pompage à usage médicalDispositifs pour retirer, traiter ou transporter les liquides du corpsSystèmes de drainage
70.
SYSTEMS AND METHODS FOR REAL-TIME PROCESSING OF MEDICAL IMAGING DATA UTILIZING AN EXTERNAL PROCESSING DEVICE
Described herein are devices for processing surgical video data associated with a surgery and methods of operating the same. An exemplary device includes a housing and a programmable circuit that is enclosed in the housing and configured to receive the surgical video data from a camera control unit. A processor is enclosed in the housing. The processor is communicatively coupled with the programmable circuit and is configured to execute a plurality of instructions for processing the video data stored on a memory. A galvanically isolated connector is exposed on the housing. The galvanically isolated connector is configured to be connected to a surgical device for contact with a patient during the surgery.
Surgical systems and methods involve a robotic manipulator and an end effector with a surgical tool configured to interact with bone. The end effector includes a compliance mechanism having a stationary portion coupled to the manipulator, a moveable portion coupled to the surgical tool, a flexible portion positioned between the stationary and moveable portions, and a sensor configured to measure displacement of the moveable portion relative to the stationary portion. A control system operates the robotic manipulator to advance the surgical tool toward the bone, receives the measured displacement produced by interaction forces applied to the surgical tool by the bone, and evaluates the displacement against a comparison condition. When the displacement indicates an error condition, the control system performs a responsive action.
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
72.
APPARATUS AND SYSTEM FOR TURNING AND POSITIONING A PATIENT
A system includes a sheet, a pad, and a first wedge. The sheet includes a bottom surface at least partially formed of a first material having a first coefficient of friction and a top surface opposite the bottom surface. The top surface includes a central portion and a peripheral portion extending about an entirety of the central portion. The central portion is at least partially formed of a second material having a second coefficient of friction that is greater than the first coefficient of friction. The pad is configured to be placed on the top surface and is formed of an absorbent material. The first wedge is configured to be placed at least partially underneath the sheet such that the sheet separates the pad from the first wedge when the pad is placed on the top surface.
A patient restraint system for restraining a patient relative to a patient transport apparatus includes an authorized patient restraint and a receiver. A latch member is supported for rotation between a lockout state to inhibit insertion of unauthorized patient restraints into the receiver, an engaged state to permit movement of the authorized patient restraint in a first direction and to inhibit movement of the authorized patient restraint in a second direction, and a disengaged state to permit movement of the authorized patient restraint in the first and second directions. A lock is configured for operation between a locked state to retain the latch member in the lockout state and an unlocked state, the lock configured to move from the locked state to the unlocked state in response to engagement of the authorized patient restraint with the receiver to release the latch member from the lockout state.
A method for creating one or more enhanced medical image includes: receiving a user interaction via a user interface, the interaction comprising a user preference for image enhancement; adjusting a combined machine learning model comprising a combination of a plurality of specialized machine learning models based on the user interaction, wherein adjusting the combined machine learning model comprises adjusting a contribution of at least one specialized machine learning model of the plurality of specialized machine learning models to the combined model; creating one or more enhanced medical images by inputting medical image data into the combined machine learning model, wherein the combined machine learning model is configured to create one or more enhanced medical images from the medical image data; and displaying the one or more enhanced medical images.
G06T 5/60 - Amélioration ou restauration d'image utilisant l’apprentissage automatique, p. ex. les réseaux neuronaux
A61B 1/00 - Instruments pour procéder à l'examen médical de l'intérieur des cavités ou des conduits du corps par inspection visuelle ou photographique, p. ex. endoscopesDispositions pour l'éclairage dans ces instruments
A system for sterilizing a wirelessly chargeable battery is provided. The system includes a wirelessly chargeable battery and a container configured to receive the wirelessly chargeable battery. The container includes a lid and a base defining a receptacle shaped to receive a wirelessly chargeable battery. The container also includes a latch assembly including a lever body and a clasp body, the lever body being movable between an unsecured position and a secured position, and the clasp body being configured to engage the base to fasten the base to the lid in the secured position.
H02J 50/00 - Circuits ou systèmes pour l'alimentation ou la distribution sans fil d'énergie électrique
A61L 2/07 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des phénomènes physiques de la chaleur des gaz chauds de la vapeur
Disclosed herein is a biocompatible composite material and a method of preparing a powder containing same. The biocompatible material can include a matrix and a second-phase dispersion. The matrix can include primary particles forming a titanium alloy. The second-phase dispersion can include secondary particles each encompassed by one of the primary particles of the matrix. The method can include preparing an ingot having the biocompatible material and atomizing the ingot to produce a composite material powder.
B22F 1/12 - Poudres métalliques contenant des particules non métalliques
B22F 9/08 - Fabrication des poudres métalliques ou de leurs suspensionsAppareils ou dispositifs spécialement adaptés à cet effet par des procédés physiques à partir d'un matériau liquide par coulée, p. ex. à travers de petits orifices ou dans l'eau, par atomisation ou pulvérisation
B33Y 70/00 - Matériaux spécialement adaptés à la fabrication additive
B22F 10/28 - Fusion sur lit de poudre, p. ex. fusion sélective par laser [FSL] ou fusion par faisceau d’électrons [EBM]
Disclosed herein are patellar implants and methods to prepare bone for receiving the same. The patellar implant may include an articulating surface with an elliptically shaped median ridge. The anterior surface of the patellar implant may have a non-planar surface to engage with a resected natural patella. The non-planar surface may allow for varying thickness of the patellar implant. The patellar implant may include dual attachment features to secure patellar implant to a resected patella by onlay and inlay techniques. A method for attaching a patellar implant to a patella may include onlay and inlay techniques and may further include bone preparation at the implant-bone interface.
A method includes determining a contour of a bone model at a cross-section intersected by a haptic object corresponding to a planned resection, the haptic object including a resection region intersecting the bone model and an approach region extending away from the resection region. The method also includes morphing the approach region of the haptic object based on the contour of the bone model. The method also includes controlling a surgical robot using the morphed haptic object, wherein the surgical robot interfaces with a cutting tool that reaches the resection region via the approach region.
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A tracking apparatus for tracking a bone of a patient limb includes a first arm and a second arm that are movable relative to one another and configured to wrap about the limb. Each arm has an exterior surface and an opposing interior surface. Ultrasonic sensors are coupled to the interior surfaces of the arms and are configured to transmit ultrasonic waves to and receive ultrasonic waves from the bone. A controller is configured to determine an integrity of contact between the arms and the limb and to generate a feedback response based on the integrity of contact.
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
80.
Mounting System With Sterile Barrier Assembly For Use In Coupling Surgical Components
A sterile barrier assembly for releasably attaching between a robotic arm and an end effector. The assembly includes a drape configured to cover the robotic arm and an interface coupled to the drape. The interface has a body with opposing first and second sides, a coupling extending through the body to provide first and second coupling interfaces, and multiple kinematic couplers extending through the body such that portions of each coupler protrude from both sides. The interface is bi-directionally mountable to the first and second mounting portions in two installation configurations. In each configuration, the coupling interfaces and kinematic coupler portions on one side engage one mounting portion, while those on the opposite side engage the other, enabling reversible connection.
An inflatable device includes a top sheet, a bottom sheet, a first port, a plurality of passages, and a plurality of gussets. The bottom sheet is coupled to the top sheet along a peripheral edge of the inflatable device. The top sheet and the bottom sheet define a cavity configured to be inflated. The first port is configured to provide access to the cavity and includes a first opening. The plurality of passages extend through the bottom sheet and are configured to permit air flow from the cavity to an exterior of the inflatable device. The plurality of gussets are coupled to the top sheet and the bottom sheet and extend across at least a portion of the cavity and divide the cavity into a plurality of sections.
A61G 7/10 - Dispositifs pour soulever les malades ou les personnes handicapées, p. ex. adaptations particulières d'appareils de levage à cet effet
A61F 13/15 - Garnitures absorbantes, p. ex. serviettes ou tampons hygiéniques pour application externe ou interne au corpsMoyens pour les maintenir en place ou les fixerApplicateurs de tampons
A61G 1/01 - Draps spécialement adaptés pour être utilisés comme ou avec des brancards
A61G 7/00 - Lits spécialement conçus pour donner des soinsDispositifs pour soulever les malades ou les personnes handicapées
A61G 7/057 - Dispositions pour éviter les escarres ou pour soutenir les patients brûlés, p. ex. matelas spécialement adaptés à cet effet
F16K 15/20 - Soupapes, clapets ou valves de retenue spécialement conçues pour corps gonflables, p. ex. les pneus
A system includes a patient support device and a positioning apparatus. The patient support device includes a first port at a first corner of the patient support device and a second port at a second corner of the patient support device. The first port is configured to coupled to an air outlet to inflate the patient support device and the second port is configured to couple to the air outlet to inflate the patient support device. The positioning apparatus includes a body. The body includes a base wall, a ramp surface, a back wall extending between the base wall and the ramp surface, and a front end opposite the back wall. The body is configured to be placed at least partially underneath the patient support device such that the ramp surface confronts a bottom surface of the patient support device.
A method of providing guidance to medical professionals with a system including electronic devices connected on a network, one or more processors, and a database storing an authoritative knowledge base. The method comprises receiving, at a first electronic device, a prompt from a first medical professional, and converting the prompt into a machine-searchable string. A trained machine learning model is directed to retrieve one or more results from the authoritative knowledge base. A query may be transmitted to a second medical professional if the trained machine learning model determines that the one or more results are not sufficiently relevant. A reply to the query from the second medical professional may be received, and the reply may be outputted on the first electronic device.
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
G16H 70/20 - TIC spécialement adaptées au maniement ou au traitement de références médicales concernant des pratiques ou des directives
G16H 80/00 - TIC spécialement adaptées pour faciliter la communication entre les professionnels de la santé ou les patients, p. ex. pour le diagnostic collaboratif, la thérapie collaborative ou la surveillance collaborative de l’état de santé
A patient support system that utilizes more than one air source in the process of inflating an inflatable bladder associated with a patient support. At least one of the air sources includes a pressure vessel or reservoir capable of storing compressed fluid, such as air.
A cable support for a mattress cable for a patient support apparatus that provides data and/or power to a mattress. The cable support may be operable to redirect a pulling force applied to a cable to a disengagement force that breaks a connection for a connector assembly without binding the connectors of the connector assembly.
A61G 7/018 - Mécanismes de commande ou d'entraînement
A61G 7/05 - Parties constitutives, détails ou accessoires de lits
H01R 13/633 - Moyens additionnels pour faciliter l'engagement ou la séparation des pièces de couplage, p. ex. moyens pour aligner ou guider, leviers, pression de gaz pour la séparation uniquement
A status unit is adapted to provide electrical power to a patient support apparatus and, in some cases, to communicate wirelessly with the patient support apparatus. In order to ensure the status unit is communicatively paired with the correct patient support apparatus, the status unit is adapted to change a voltage of the power supplied to the patient support apparatus in a manner that matches a power pattern, as well as to wirelessly transmit a message to the patient support apparatus that includes the power pattern. The patient support apparatus is adapted to sense the power received from the status unit, determine if it matches the power pattern and, if it does, pair with the status unit. If it does not match the power pattern, the patient support apparatus does not pair with the status unit. The power pattern may include a series of power-off intervals.
A61G 7/05 - Parties constitutives, détails ou accessoires de lits
G08B 26/00 - Systèmes d'alarme dans lesquels des sous-stations sont interrogées successivement par une station centrale
G16H 40/40 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion d’équipement ou de dispositifs médicaux, p. ex. pour planifier la maintenance ou les mises à jour
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
G06F 13/38 - Transfert d'informations, p. ex. sur un bus
H02J 50/80 - Circuits ou systèmes pour l'alimentation ou la distribution sans fil d'énergie électrique mettant en œuvre l’échange de données, concernant l’alimentation ou la distribution d’énergie électrique, entre les dispositifs de transmission et les dispositifs de réception
H04B 1/3877 - Dispositions permettant l’utilisation d’émetteurs-récepteurs portables dans une position fixe, p. ex. par des berceaux ou des boosters
H04B 5/79 - Systèmes de transmission en champ proche, p. ex. systèmes à transmission capacitive ou inductive spécialement adaptés à des fins spécifiques pour le transfert de données en combinaison avec le transfert d'énergie
H04W 12/63 - Sécurité dépendant du contexte dépendant de la localisationSécurité dépendant du contexte dépendant de la proximité
H04W 36/32 - La resélection étant déclenchée par des paramètres spécifiques par des données de localisation ou de mobilité, p. ex. des données de vitesse
H04W 76/27 - Transitions entre états de commande de ressources radio [RRC]
H04W 88/04 - Dispositifs terminaux adapté à la retransmission à destination ou en provenance d'un autre terminal ou utilisateur
H04W 88/12 - Dispositifs contrôleurs de points d'accès
88.
MODIFIABLE LOCATION SYSTEM AND DISPLAY SYSTEM FOR A HEALTHCARE FACILITY
A location beacon for determining the location of patient support apparatuses and/or other devices in a healthcare facility includes a housing, display, memory, wireless transceiver, and controller. The housing is detachably mounted to a wall. The display visually displays a location indicator (e.g. "East Corridor") indicative of the beacon's location. The memory includes a unique ID. The wireless transceiver communicates with a patient support apparatus and/or other mobile device. The controller transmits the ID to the patient support apparatus or other mobile device when it is within a threshold distance. The display may be an electronic ink display. The location indicator may be changed via direct interaction with the location beacon, via coupling a computer or cell phone thereto, via the patient support apparatus, and/or via a server. The location beacon is movable to another location and its location indicator is easily updated to match its new location.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
G16H 40/60 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux
89.
Methods For Characterizing Fluids Flowing Through A Conduit With A System Including Optical Emitters And Detectors
Systems and methods for characterizing fluid through a conduit. The conduit may be noncircular, and a sensor module may include emitters and detectors spaced apart from one another by different distances such that light signals travel through the non-circular conduit in longer and shorter paths. The emitters may be alternatingly fired, or a second emitter may be fired if the light signal detected by a first detector is below a sensitivity threshold. More than two emitters and detectors may be provided for which a data rich matrix is provided based on absorbance and scatter values from each of the detectors in combination with each of the emitters. The travel paths and/or angles of the various combinations of emitters and detectors may be different. The data rich matrix may be provided to a machine-trained neural network to implement an algorithm to determine fluidic components within the fluid.
G01N 21/31 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes en recherchant l'effet relatif du matériau pour les longueurs d'ondes caractéristiques d'éléments ou de molécules spécifiques, p. ex. spectrométrie d'absorption atomique
A61M 1/00 - Dispositifs de succion ou de pompage à usage médicalDispositifs pour retirer, traiter ou transporter les liquides du corpsSystèmes de drainage
G01N 21/85 - Analyse des fluides ou solides granulés en mouvement
G01N 33/49 - Analyse physique de matériau biologique de matériau biologique liquide de sang
A patient support apparatus system includes one or more patient support apparatuses, one or more location beacons, and, in some instances, a server. Each patient support apparatus includes a wireless transceiver adapted to range with the location beacon(s) to determine position information. The location beacon(s) transmit movement data, such as intersection data, corner data, speed limit data, and/or other data to the patient support apparatus. The patient support apparatus includes one or more powered wheels and it uses the movement data for controlling movement of the powered wheel and/or assisting the user of the patient support apparatus in the movement of the patient support apparatus. In some versions, the location beacon and/or server may be used to map areas of the healthcare facility where impacts above a threshold commonly occur, thereby allowing the patient support apparatus to automatically mitigate the impact forces during future visits to those areas.
A61G 1/04 - Parties constitutives, détails ou accessoires, p. ex. appuis-tête, repose-pied, éléments d'appui ou analogues, spécialement adaptés aux brancards
A headband of a surgical helmet including an electrically powered assembly, the headband including a front portion, a rear portion and opposed side portions connecting the front portion to the rear portion. The rear portion of the headband including a base member, a pair of contact surfaces, and at least one support member disposed between each of the pair of contact surfaces and the base member. The base member slidably receiving each of the opposed side portions of the headband. The contact surfaces being spaced apart from one another to define a first void therebetween and configured to contact the head of the wearer. The support member configured to offset the contact surface from the base member to define a second void between each of the pair of contact surfaces and the base member of the rear portion of the headband.
An embolic hydrogel for use with a patient comprise an aqueous buffer and at least one functionalized polymer respectively having at least one polymer backbone chemically modified with one or more functional groups. The functional group(s) facilitate formation of primary reversible crosslinks on the polymer backbone(s), such that the embolic hydrogel transitions from a gel state to a viscous liquid state in response to a shear force applied to the embolic hydrogel, and transitions from the viscous liquid state back to the gel state in response to an absence of a shear force applied to the embolic hydrogel. The embolic hydrogel further comprises at least one phase-transitioning polymer that creates secondary crosslinks therein in response to a physiological environment, such that the embolic hydrogel transitions from the gel state to a solid state.
A61B 17/12 - Instruments, dispositifs ou procédés chirurgicaux pour ligaturer ou comprimer par un autre moyen les parties tubulaires du corps, p. ex. les vaisseaux sanguins ou le cordon ombilical
A61L 24/00 - Adhésifs ou ciments chirurgicauxAdhésifs pour dispositifs de colostomie
A61L 24/02 - Adhésifs ou ciments chirurgicauxAdhésifs pour dispositifs de colostomie contenant des matériaux inorganiques
A61L 24/04 - Adhésifs ou ciments chirurgicauxAdhésifs pour dispositifs de colostomie contenant des matériaux macromoléculaires
In an example, a fecal collection system includes a user interface assembly, a drainage conduit, and a collection reservoir. The user interface assembly includes a user interface and an applicator. The user interface has a proximal side and a distal side. The proximal side is configured to couple to skin of a user. The applicator is coupled to the distal side of the user interface. The applicator is removable from the user interface while the user interface is coupled to the user. The drainage conduit extends between a proximal end and a distal end. The proximal end is configured to couple to the distal side of the user interface. The drainage conduit defines a lumen configured to guide feces from the proximal end to the distal end. The collection reservoir coupled to the distal end of the drainage conduit.
A61F 5/448 - Moyens d'assujettissement du sac à l'anneau d'étanchéité
A61F 5/44 - Dispositifs portés par le patient pour recueillir l'urine, les selles, les menstrues ou d'autres sécrétionsDispositifs de colostomie
A61F 5/443 - Dispositifs portés par le patient pour recueillir l'urine, les selles, les menstrues ou d'autres sécrétionsDispositifs de colostomie comportant des joints d'étanchéité de type hydrocolloïde, p. ex. gels, empois d'amidon, gomme Karaya
An applicator device configured for delivery of at least one solution to a surface, includes an applicator body having a head portion including an opening, a distal end, and an outer wall forming an interior space, and a fluid container moveably positioned in the interior space of the applicator body, the fluid container having an interior portion for holding the at least one solution and a membrane for preventing passage of the solution out of the interior portion. The device further includes a piercing element configured to breach the membrane to allow for passage of the solution out of the interior space of the fluid container, and a distal cap coupled to the distal end of the applicator body configured such that rotation of the distal cap causes longitudinal movement of the fluid container within the interior space of the applicator body into contact with the piercing element.
A system including a monitoring system, a patient transport apparatus having and a track assembly with a belt for engaging stairs, and a loading device configured to engage the patient transport apparatus for loading and unloading from a transport vehicle. The loading device includes a stage, a receiver arranged for translational movement relative to the stage between a lowered position and a raised position, and a dock operatively attached to the receiver for supporting the patient transport apparatus. The monitoring system includes a monitor controller in communication with a sensing system for monitoring the loading device is configured to activate an output device arranged remotely from the loading device in response to one or more signals received from the sensing system satisfying a predetermined condition for communicating a status of the loading device to a caregiver.
A61G 5/06 - Fauteuils ou moyens de transport personnels spécialement adaptés pour des personnes handicapées, p. ex. fauteuils roulants avec dispositions pour franchir les obstacles, p. ex. pour monter les escaliers
A61G 3/08 - Logement ou immobilisation des chaises roulantes
A system for monitoring compliance with desired operating parameters of patient support apparatuses in a healthcare facility includes a patient support apparatus and a server. The patient support apparatus forwards status data and occupancy data to the server indicating which state each of a plurality of components is currently in, and whether the patient is currently occupying the patient support apparatus. The server is adapted to receive admission data indicating whether the patient has been admitted or discharged from the healthcare facility, determine whether the patient support apparatus is in a use state, determine if a plurality of components are in their desired states, and determine an overall compliance value. The use state may be defined by the patient support apparatus being occupied, the patient being admitted, and a fall risk being assigned to the patient. The system may alternatively or additionally compute individual compliance values for the individual components.
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
G16H 15/00 - TIC spécialement adaptées aux rapports médicaux, p. ex. leur création ou leur transmission
G16H 40/20 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion ou l’administration de ressources ou d’établissements de soins de santé, p. ex. pour la gestion du personnel hospitalier ou de salles d’opération
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
A61G 7/015 - Lits spécialement conçus pour donner des soinsDispositifs pour soulever les malades ou les personnes handicapées comportant un cadre de sommier réglable divisé en plusieurs parties réglables, p. ex. pour la position dite "Gatch"
09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
non-downloadable software for inventory management and optimization software as a service (SAAS) featuring software for inventory management and optimization
