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BRAKE ASSEMBLY, STEERING ARM ASSEMBLY AND RACING WHEELCHAIR

Publication No.:  US20260077746A1 19/03/2026
Applicant: 
RGK WHEELCHAIRS LTD [GB]
RGK Wheelchairs Ltd
US_20260077746_A1

Absstract of: US20260077746A1

A brake assembly for a personal mobility vehicle, in form of a racing wheelchair, comprises a brake lever for actuating a brake cable, wherein the brake lever is a 3D printed glass filled nylon unit, in particular with up to 30% glass filled nylon. A steering arm assembly comprises a steering arm with the brake assembly integrated into the steering arm A racing wheelchair with one front wheel is attached to a wheelchair frame via a fork, with two drive wheels as well as a steering cage mounted on the rear of the wheelchair frame. The brake assembly and/or the steering arm assembly are mounted to the wheelchair frame.

SYSTEMS AND METHODS FOR DENTURE INJECTION MOLD DESIGN AND MANUFACTURE

Publication No.:  WO2026060305A1 19/03/2026
Applicant: 
ZIMA INT INC D/B/A DANDY [US]
MOORE PATRICK R [US]
BUTLER KENN [US]
WAINWRIGHT SAMUEL [US]
WO_2026060305_A1

Absstract of: WO2026060305A1

The present disclosure provides a method for generating a dental appliance injection model. The method comprises receiving a three-dimensional (3D) dental model representing a dental appliance, detecting a parting direction of a mold of the dental model, generating a parting line around a perimeter of the 3D dental model using a first executable algorithm, generating a parting surface for the dental model using a second executable algorithm, and generating a first digital representation of a first mold component and a second digital representation of a second mold component aligned with the parting line, wherein the first mold component and the second mold component define a mold cavity.

HYDROGELS FOR 3D PRINTING HAVING HIGH RESOLUTION

Publication No.:  US20260078274A1 19/03/2026
Applicant: 
3D SYSTEMS INC [US]
3D SYSTEMS, INC
US_20260078274_A1

Absstract of: US20260078274A1

In one aspect, build materials for use with a three-dimensional (3D) printing system are described herein. In some embodiments, a build material described herein comprises an acrylate component, a photoinitiator component, a non-curable absorber component, and water. The photoinitiator component of the build material is operable to initiate curing of the acrylate component and/or other curable materials that may optionally be present when the photoinitiator is exposed to incident curing radiation having a Gaussian distribution of wavelengths and a peak wavelength λ. The build material has a penetration depth (Dp) and a critical energy (Ec) at the wavelength λ. In some embodiments, the Dp is greater than 200 μm and less than 300 μm, and the Ec is 3-12 mJ/cm2. In other embodiments, the Dp is greater than 10 μm and less than 50 μm, and the Ec is 5-40 mJ/cm2.

BIOMEDICAL TEST FOR AUTISM

Publication No.:  US20260079167A1 19/03/2026
Applicant: 
UNIV ARIZONA STATE [US]
RENSSELAER POLYTECH INST [US]
US_20260079167_A1

Absstract of: US20260079167A1

0000 Diagnostic metabolites and methods of using the metabolites for the diagnosis of autism spectrum disorder (ASD) are provided. The metabolites comprise a collection of 47 metabolites that were significantly different between the autistic and typically developing groups, and combinations of two or more of the metabolites are used to accurately diagnose ASD.

MEDICAL DEVICE DATA BACK-ASSOCIATION, SYSTEM, APPARATUSES, AND METHODS

Publication No.:  US20260080990A1 19/03/2026
Applicant: 
BAXTER INT [US]
BAXTER HEALTHCARE SA [CH]
US_20260080990_A1

Absstract of: US20260080990A1

0000 A medical device data back-association system, apparatuses, and methods are disclosed. In an example embodiment, a server receives, while an infusion pump is administering a medication to a patient, an identifier message including at least two of a device identifier of the infusion pump, a patient identifier of the patient, and a medication order identifier of a medication being administered by the infusion pump. The server prompts a clinician device for creating an association between an electronic medical record (“EMR”) of the patient and the infusion pump. When an association to be created, the server uses contents of the identifier message to create the association. For subsequently received infusion pump data, the server stores this infusion pump data to the EMR of the patient based on the created association between the EMR of the patient and the infusion pump.

CRYO-ASSISTED IRREVERSIBLE ELECTROPORATION (IRE) ABLATION SYSTEM AND METHOD

Publication No.:  WO2026058249A1 19/03/2026
Applicant: 
BERGER ABRAHAM [IL]
HAZAN ORI EMANUEL [IL]
WO_2026058249_A1

Absstract of: WO2026058249A1

The cryo-assisted Irreversible Electroporation (IRE) ablation system includes an IRE ablation generator, a coolant supply, cryo-assisted IRE ablation stylet(s), and a cryo-assisted IRE ablation controller for controlling the IRE ablation generator and the cryo-assisted IRE ablation stylet(s). The ablation stylets include a stylet needle having longitudinally directed strip electrode(s) and a freezing module for cooling a longitudinal directed ice-forming surface for freezing a generally hemi-ellipsoidal volume of target tissue. The controller repeatedly switches the ablation stylets between an IRE ablation energy mode and a non-cryoablation freezing mode whereupon, in an absence of ice formation, each cryo-assisted IRE ablation stylet generates a pre-ice 3D electric field pattern in target tissue and, subsequent to a generally hemi-ellipsoidal ice formation, the ice formation modifies the pre-ice 3D electric field pattern to a post-ice 3D electric field pattern different from the pre-ice 3D electric field pattern.

Clip zur Befestigung an einem saugfähigen Artikel

Publication No.:  DE102024004559A1 19/03/2026
Applicant: 
ASSISTME GMBH [DE]
DE_102024004559_PA

Absstract of: DE102024004559A1

Die Erfindung betrifft einen Clip (1) zur Befestigung an einem saugfähigen Artikel (4). Der Clip (1) umfasst eine Leiterplatte (2), PCB, ein Gehäuse (11), das ein schwenkbares Oberteil (111), ein mit dem Oberteil (111) an einer Faltkante (113) verbundenes schwenkbares Unterteil (112) und ein zwischen dem Oberteil (111) und dem Unterteil (112) angeordnetes Mittelteil (114) aufweist, wobei Unterteil (112) und Mittelteil (114) einen Hohlraum (115) für die PCB (2) bilden, wobei Oberteil (111) und Unterteil (112) um die Faltkante (113) zwischen einer geschlossenen und einer geöffneten Position des Gehäuses (11) schwenkbar sind. Das Unterteil (112) umfasst eine Sensorkammer (116) für ein Gaserfassungsmodul (22) und eine mit einer semipermeablen Membran (12) abgedeckte Öffnung zum Abdichten gegen Flüssigkeiten und zum Durchlassen von Gasen, wobei die Sensorkammer (116) eine nach innen gerichtete Extrusion im Gehäuse (11) für eine schnellere Reaktion, eine schnellere Erholungszeit und eine höhere Präzision des Gaserfassungsmodul (22) umfasst. Der Clip (1) umfasst ferner im Mittelteil (114) angeordnete Pogo-Pins (13), die mit der PCB (2) elektrisch verbunden sind und mit einer Energiequelle, mit einem eingebetteten externen Messmittel (43) und/oder mit dem externen Gerät elektrisch verbindbar sind, und eine ein Innenvolumen des Gehäuses (11) umgebende und das Unterteil (112) und das Mittelteil (114) berührende Dichtung (14) zum Abdichten des Hohlraums (115).

BIOCOMPATIBLE PRINTABLE POLY-MMA-EGDMA RESINS FOR ORTHOPEDIC IMPLANTS

Publication No.:  WO2026060380A2 19/03/2026
Applicant: 
SAN DIEGO STATE UNIV SDSU FOUNDATION DBA SAN DIEGO STATE UNIV RESEARCH FOUNDATION [US]
WO_2026060380_A2

Absstract of: WO2026060380A2

Systems and methods for additive-manufactured biocompatible implants. Many embodiments are directed to 30-printed biocompatible resins for fabricating custom implants. In several embodiments, the biocompatible resin is based on a ratio of biocompatible polymers. The biocompatible resin, in accordance with various embodiments, incorporates an antibacterial and/or antimicrobial agent, In some embodiments, the biocompatible resin incorporates a bioceramic to mimic native tissue.

INFUSION VOLUME DETECTION SYSTEM AND METHOD

Publication No.:  AU2024434464A1 19/03/2026
Applicant: 
CAREFUSION 303 INC [US]
AU_2024434464_A1

Absstract of: AU2024434464A1

A vision-enabled fluid flow rate detection system is disclosed. The system includes an image sensing device that images an infusion container supplying a fluid to an infusion pump and a pattern of markings associated with a surface of the container, and identifies a visual difference in the pattern from a default state of the pattern to determine a volume of fluid infused from the infusion container, and used to calculate a volume of fluid in the container and a flow rate of the fluid. When the amount of fluid, as determined by the vision system, differs from the amount reported by the pump, the pump's motor may be adjusted to correct the expected volume or flow rate, as needed. When a severe infusion inaccuracy is detected, an alarm or other indication may be provided, or the infusion terminated.

ADJUDICATING REMOTE PROGRAMMING INSTRUCTIONS

Publication No.:  WO2026059852A1 19/03/2026
Applicant: 
CARDIAC PACEMAKERS INC [US]
WO_2026059852_A1

Absstract of: WO2026059852A1

Systems and methods are disclosed for adjudicating instructions prior to programming an ambulatory medical device to optimize resources of the ambulatory medical device, including receiving a programming instruction for the ambulatory medical device generated at a first time, implementing adjudication of the programming instruction to optimize resources of the ambulatory medical device, and suspending the received programming instruction or programming the ambulatory medical device based on the adjudication to optimize resources of the ambulatory medical device.

CENTRALIZED HUB DEVICE FOR DETERMINING AND DISPLAYING HEALTH-RELATED METRICS

Publication No.:  US20260076616A1 19/03/2026
Applicant: 
SLEEP NUMBER CORP [US]
US_20260076616_A1

Absstract of: US20260076616A1

Described are systems for beds that can include sensors for sensing physical phenomena in an environment surrounding a bed, a display for outputting information about the environment, the bed, and a sleeper, and a controller communicably coupled to the sensors. The controller can receive the sensed physical phenomena from the sensors, analyze the physical phenomena to determine at least one of environmental, sleep, and health metrics of a sleeper in the bed, and determine, based on at least one of the environmental, sleep, and health metrics of the sleeper, control signals to modify the environment surrounding the bed. The controller can also output, at the display, the environmental, sleep, and health metrics of the sleeper. The controller can also transmit the control signals to a second controller in order to engage a home automation device. The physical phenomena can include ambient sound, ambient light, ambient CO2 concentration, and/or ambient temperature.

Extended Intelligence for Pulmonary Procedures

Publication No.:  US20260076746A1 19/03/2026
Applicant: 
MEDTRONIC INC [US]
US_20260076746_A1

Absstract of: US20260076746A1

A computing system receives pre-procedural work-up data of a patient for a pulmonary procedure. A computing system receiving disease trigger data for the patient. A computing system analyzes, via an artificial intelligence algorithm, the received pre-procedural work-up data and the received disease trigger data. A computing system generates recommendations for assisting a medical professional in performing the pulmonary procedure based on the analysis, wherein the recommendations include a device specification for a device, a device trajectory for the device, a target location, and procedural steps for the pulmonary procedure. A computing system generates extended reality (“XR”) images, based on the recommendations. A computing system presents, using a user experience (“UX”) device, the XR images that aid in placement of the device.

投与機器

Publication No.:  JP2026050505A 19/03/2026
Applicant: 
ベクトン・ディキンソン・アンド・カンパニー
JP_2026050505_A

Absstract of: EP1000000A1

The invention relates to an apparatus (1) for manufacturing green bricks from clay for the brick manufacturing industry, comprising a circulating conveyor (3) carrying mould containers combined to mould container parts (4), a reservoir (5) for clay arranged above the mould containers, means for carrying clay out of the reservoir (5) into the mould containers, means (9) for pressing and trimming clay in the mould containers, means (11) for supplying and placing take-off plates for the green bricks (13) and means for discharging green bricks released from the mould containers, characterized in that the apparatus further comprises means (22) for moving the mould container parts (4) filled with green bricks such that a protruding edge is formed on at least one side of the green bricks.

UNIVERSAL TISSUE FABRICATION TECHNIQUES FOR SELF-ASSEMBLED ORGAN PRODUCTION AND REGENERATIVE MEDICINE APPLICATIONS

Publication No.:  WO2026060262A1 19/03/2026
Applicant: 
FRONTIER BIO CORP [US]
BENNETT ERIC [US]
BUDDHIKOT OMKAAR [US]
GRUBER VICTORIA ELISABETH [US]
GOMES NIGEL [US]
VALDOZ JONARD [US]
FRONTIER BIO CORPORATION,
BENNETT, Eric,
BUDDHIKOT, Omkaar,
GRUBER, Victoria-Elisabeth,
GOMES, Nigel,
VALDOZ, Jonard
WO_2026060262_A1

Absstract of: WO2026060262A1

Methods and systems are described for a high-level approach to organ generation by self-assembly using bioprinting, overcoming longstanding challenges in replicating the intricate architecture and function of complex organs. In some embodiments, these methods are used to produce lung tissues and microtissues, demonstrating how mini-lung constructs can be produced on a small scale through specialized processes and media. In such embodiments, methods and systems for generating bioprinted lung tissues and microtissues are provided, as are tissues made by such methods. The tissues find use in implantation, drug discovery, personalized medicine, and other applications. Methods for the large-scale manufacturing of lung epithelial stem cells are also provided.

STREAMLINED AND AUTOMATIC EVALUATION OF VISION CHANGES

Publication No.:  US20260076550A1 19/03/2026
Applicant: 
ZENNI OPTICAL INC [US]
US_20260076550_A1

Absstract of: US20260076550A1

An eye exam can be performed using an electronic device in a virtual environment to evaluate vision changes of a patient. The electronic device can execute a visual assessment application and display a user interface to create a 3D virtual environment. A predefined video clip can be displayed in the 3D virtual environment and include a plurality of visual sessions corresponding to a sequence of vision tests. While the predefined video clip is played, the electronic device can obtain a stream of sensor data measured by the one or more sensors and determine a plurality of first response parameters to the sequence of vision tests based on the stream of sensor data.

DETERMINATION OF VISUAL SUSCEPTIBILITY TO DIGITAL SCREEN USE

Publication No.:  US20260076559A1 19/03/2026
Applicant: 
ZENNI OPTICAL INC [US]
US_20260076559_A1

Absstract of: US20260076559A1

0000 An eye exam can be performed using an electronic device in a virtual environment to determine visual susceptibility to digital screen use. The electronic device can execute a visual assessment application and display a user interface to create a 3D virtual environment. Visual content can be continuously displayed for an extended duration of time with predefined display parameters associated with a screen usage in the 3D virtual environment. The electronic device can obtain a stream of sensor data measured by the one or more sensors and determine a plurality of sequential user responses to the visual content based on the stream of sensor data. The electronic device can apply at least a screen usage prediction model to generate a screen usage guidance profile for the user based on the plurality of sequential user responses.

CONTENT RENDERING FOR MULTIFOCAL EYEWEAR FITTING

Publication No.:  US20260076548A1 19/03/2026
Applicant: 
ZENNI OPTICAL INC [US]
US_20260076548_A1

Absstract of: US20260076548A1

0000 A multifocal eyewear fitting procedure can be performed using an electronic device in a virtual environment. The electronic device can execute a visual assessment application and display a user interface to create a 3D virtual environment. A comprehensive prescription for an eyewear can have a plurality of lens portions, and each lens portion may correspond to a distinct region of a field of view and have a respective prescription parameter. The electronic device can generate a bifocal filter, a trifocal filter, and/or a progressive filter based on the comprehensive prescription. The electronic device can obtain 3D visual content for display on the user interface and render a plurality of versions of the first 3D visual content based on the bifocal filter, the trifocal filter, and/or the progressive filter.

MACHINE-LEARNING-BASED CONTACT LENS FITTING ANALYSIS

Publication No.:  US20260076551A1 19/03/2026
Applicant: 
ZENNI OPTICAL INC [US]
US_20260076551_A1

Absstract of: US20260076551A1

A patient's contact lens fitting profile can be performed using an electronic device in a virtual environment. The electronic device can execute a visual assessment application and display visual content continuously for an extended duration of time in the 3D virtual environment. The visual content can be displayed with predefined display parameters associated with contact lens fitting. The electronic device can obtain a stream of sensor data measured by the one or more sensors and apply at least a contact lens fitting model to generate a contact lens fitting profile for a user associated with the electronic device based on the stream of sensor data.

IMAGE-BASED PAIRING AND CONTROLLING OF DEVICES IN A CLINICAL ENVIRONMENT

Publication No.:  US20260076849A1 19/03/2026
Applicant: 
HILL ROM SERVICES INC [US]
US_20260076849_A1

Absstract of: US20260076849A1

An example method includes capturing images using a camera and detecting a medical device in a first image among the images. A request is transmitted to the medical device. Based on transmitting the request, the example method includes determining that the medical device has output a chirp signal in a second image among the images. Based on the chirp signal, the method includes causing the medical device to perform an action by transmitting a control message to the medical device.

SYSTEMS, METHODS, AND DEVICES FOR TRACKING SURGICAL INSTRUMENTS AND DEVICES

Publication No.:  US20260076770A1 19/03/2026
Applicant: 
SMADE S A S [FR]
US_20260076770_A1

Absstract of: US20260076770A1

0000 Surgical instrument tracking systems, methods and devices are described. The system can include tracking devices configured to detect location events. The tracking device can include sensors, circuits, power sources, memories, and radio interface. The tracking devices can automatically determine a location of the tracking device when the tracking device detects a location event. The tracking device can automatically transmit the location and information related to the location event to a data analytics platform. The data analytics platform can allow a user to track multiple surgical instruments and surgical instrument tray in order to accurately determine when surgical instruments should be replaced, and how efficiently the surgical instruments are used.

Systems and methods for patient monitoring using an HCP-specific device

Publication No.:  AU2026201602A1 19/03/2026
Applicant: 
DEXCOM INC [US]
AU_2026201602_A1

Absstract of: AU2026201602A1

Systems and methods disclosed provide ways for Health Care Professionals (HCPs) to be involved in initial patient system set up so that the data received is truly transformative, such that the patient not just understands what all the various numbers mean but also how the data can be used. For example, in one implementation, a CGM device is configured for use by a HCP, and includes a housing and a circuit configured to receive a signal from a transmitter coupled to an indwelling glucose sensor. A calibration module converts the received signal into clinical units. A user interface is provided that is configured to display a measured glucose concentration in the clinical units. The user interface is further configured to receive input data about a patient level, where the input data about the patient level causes the device to operate in a mode appropriate to the patient level. ar a r

METHODS AND SYSTEMS FOR NEURAL STIMULATION VIA VISUAL, AUDITORY AND PERIPHERAL NERVE STIMULATIONS

Publication No.:  US20260077210A1 19/03/2026
Applicant: 
COGNITO THERAPEUTICS INC [US]
US_20260077210_A1

Absstract of: US20260077210A1

0000 Systems and methods of the present disclosure are directed to systems and methods for treating cognitive dysfunction in a subject in need thereof. The system can include a light source and a speaker. A visual neural stimulation system provides, via the light source, visual stimulation having a first value of a first parameter. An auditory neural stimulation system provides, via the speaker, audio stimulation having a second value of the second parameter. A stimuli orchestration component selects, for a first time interval, one of the visual stimulation or the audio stimulation to vary based on a policy, selects, for the first time interval, the other of the visual stimulation or the audio stimulation to keep constant based on the policy, and provides causes the one of the visual neural stimulation system or the auditory neural stimulation system to vary the one of the visual stimulation or the audio stimulation.

DETERMINATION OF CORRECTIVE MEASURES BASED ON VISION CORRECTION SIMULATION

Publication No.:  US20260076549A1 19/03/2026
Applicant: 
ZENNI OPTICAL INC [US]
US_20260076549_A1

Absstract of: US20260076549A1

0000 An eye exam can be performed using an electronic device in a virtual environment to determine vision corrective measures based on vision correction simulation. The electronic device can execute a visual assessment application for displaying a user interface to create a 3D virtual environment corresponding to a field of view of a user associated with the electronic device. The electronic device can render a visual pattern in the field of view and apply a vision correction filter to the visual pattern. The electronic device can obtain a set of user response data captured by a plurality of sensors in response to the visual pattern and determine whether the set of user response data satisfy a response quality criterion. Filter parameters of the vision correction filter can be dynamically adjusted based on the set of user response data until the set of user response data satisfy the response quality criterion.

MULTI-REGION EYEWEAR PRESCRIPTION

Publication No.:  US20260076542A1 19/03/2026
Applicant: 
ZENNI OPTICAL INC [US]
US_20260076542_A1

Absstract of: US20260076542A1

0000 An eye exam can be performed using an electronic device in a virtual environment to provide a corrective vision prescription covering a field of view. The electronic device can execute a visual assessment application, e.g., by displaying a user interface to create a 3D virtual environment. The electronic device can partition a field of view displayed on the user interface into a plurality of regions. For each of the plurality of regions in the field of view, successively, the electronic device can render a respective visual pattern in the respective region, obtain a user response to the respective visual pattern, and adjust a respective vision correction filter to the respective visual pattern based on the user response. Respective vision correction filters corresponding to the plurality of regions are combined to determine a prescription of an eyewear for a user associated with the electronic device.

DETERMINATION OF SIGHTLINE-BASED CORRECTIVE MEASURES OF EYEWEAR

Nº publicación: US20260076546A1 19/03/2026

Applicant:

ZENNI OPTICAL INC [US]

US_20260076546_A1

Absstract of: US20260076546A1

An eye exam can be performed using an electronic device in a virtual environment to determine corrective measures of an eyewear based on sightlines. The electronic device can execute a visual assessment application and display a user interface to create a 3D virtual environment. The electronic device can identify a plurality of horizontal lines of sight. For each horizontal line of sight, the electronic device can render a respective visual stimulus on the respective horizontal line of sight, obtain a user response to the respective visual stimulus, and dynamically adjust stimulus parameters of the respective visual stimulus based on the user response. Based on the stimulus parameters associated with each horizontal line of sight, an eyewear prescription of an eyewear can be determined for a user associated with the electronic device. The eyewear prescription can include prescription parameters corresponding to the plurality of horizontal lines of sight.

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