Resumen de: JP2025069416A
To provide systems and methods that include a monitoring interval tracker for managing transmission data originating from a cardiac monitoring device.SOLUTION: A monitoring interval tracker generates monitoring intervals corresponding to multiple, different patient care modalities (for example, an in-office care modality, a remote monitoring care modality, and/or a heart failure care modality). Upon receiving transmission data, a docket report corresponding to the transmission data, and/or an approval of the docket report, the monitoring interval tracker determines whether to extend the monitoring interval, generate a date of service, and/or create a new monitoring interval. Multiple monitoring intervals may run concurrently to track transmission data, docket reports, and approval time-stamps for the multiple, different patient care modalities. Results of the monitoring interval tracker may be outputted as an interactive monitoring interval visualizer and/or a transmission dashboard to improve patient care by preventing failures to follow up with patients and by improving billing accuracy and efficiency.SELECTED DRAWING: Figure 1
Resumen de: 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.
Resumen de: EP3971776A1
0001 This medical container (1) comprises a tubular barrel (10) defining a reservoir for a medical product. The barrel (10) is provided with a scale (14) having graduations indicative of an injected volume or a remaining volume of said medical product. The barrel (10) further comprises a RFID tag (4) including an antenna (42) that forms, follows or overlays with at least a portion of the scale (14).
Resumen de: CN114830252A
A server is provided and is programmed to automatically determine whether there is an upgrade to code or data (e.g., software or firmware) stored in electronic memory of a patient device, to which the upgrade may be applied, based on identification data uniquely identifying the patient device. In response to determining that there is an applicable upgrade, a data packet is transmitted to the patient device via the first wireless transceiver, the data packet to be automatically applied to an electronic memory of the patient device.
Resumen de: US11134880B2
Disclosed is a method for computerizing delineation and/or multi-label classification of an ECG signal, including: applying a neural network to the ECG, labelling the ECG, and optionally displaying the labels according to time with the ECG signal.
Resumen de: CN121818118A
本发明提供一种可读存储介质及骨科机器人系统,可读存储介质上存储有程序,程序被执行时实现如下步骤:基于股骨假体的公开参数,在目标股骨的术前医学影像或三维模型上设置特征参考点,以确定远端面和后髁面的截骨参考基准;在目标股骨上执行远端面和后髁面的截骨,形成远端截骨面和后髁截骨面;基于后髁截骨面,安装定位导向装置,使定位导向装置贴靠于后髁截骨面;将截骨板配合安装于定位导向装置,使截骨板贴靠于远端截骨面;基于截骨板的引导,完成前髁面、前斜面和后斜面三个面的截骨。如此配置,不受限于假体产品公司授权膝关节假体的完整几何参数,可实现开放式的膝关节假体互换选择,不受限于使用特定品牌的假体产品。
Resumen de: US20260096877A1
Disclosed are apparatus and methods for 3D printing intraocular lens components, intraocular lens formulations suitable for 3D printing, and 3D-printed intraocular lens components. In one aspect, the intraocular lens formulation can comprise a plurality of monomers, a crosslinkable polymer comprising the plurality of monomers, a crosslinker, and a photoinitiator. Also disclosed is a 3D printer for printing an intraocular lens component. The 3D printer can comprise a reservoir configured to contain an intraocular lens formulation, a build platform comprising a build surface configured to be initially in fluid contact with the intraocular lens formulation within the reservoir, a light source configured to generate a light, and at least one of a mirror and a projection optic configured to direct the light generated by the light source at the intraocular lens formulation within the reservoir to cure and form one layer of the intraocular lens component on the build surface.
Resumen de: US20260096869A1
0000 A method of designing a patient removable tooth positioning appliance may include receiving a digital representation of teeth of the patient in a selected arrangement and modeling the patient removable tooth positioning appliance having tooth receiving cavities shaped to receive and apply a resilient positioning force to the teeth of the patient based on the digital representation. The method may also include modeling a hook integral to the patient removable tooth positioning appliance and configured to interface with an elastic member so as to react a force from the elastic member into the appliance. The hook may be configured to be laterally offset from a portion of a tooth receiving cavity of the tooth receiving cavities. The method may also include outputting a three-dimensional representation of the patient removable tooth positioning appliance having the hook for fabrication by one or more fabrication machines.
Resumen de: US20260096823A1
Disclosed herein is a disposable patella clamp. In some examples, the patella clamp is configured as a patient specific patella clamp that is custom designed to fit the anatomy of a particular patient. A patient undergoes diagnostic imaging which provides patient specific data including patella diameter and thickness, patella shape, and limb alignment. The imaging can be used to generate a 3D digital model of the patient's anatomy associated with the patellar region. The patella clamp can be designed and manufactured based on the model as an integrated clamp using an additive manufacturing process with biocompatible materials. The patella clamp may include one or more tracking elements operative to enable the patella clamp to be used with a computer-assisted and/or robotic surgical system.
Resumen de: US20260096729A1
Systems, devices, and methods including a processor having addressable memory, where the processor is configured to: generate a series of recordings using a plurality of sensors via receiving a set of full measurements at a scheduled recording time; assign a priority to each of the recordings based on detection of abnormalities; determine a new recording schedule based on the generated series of recordings and detected abnormalities in the processed series of recordings; transmit the generated series of recordings and associated flag indicating whether an abnormality is present in the generated series of recordings; determine abnormal health patterns based on continuous monitoring capabilities; and provide an alert about the abnormal health patterns.
Resumen de: US20260096880A1
0000 A system for transesophageal echocardiogram-guided implantation of a valve device, the system including at least a transesophageal echocardiogram system configured to detect at least an ultrasound image and at least a computing device configured to receive at least an ultrasound image, generate at least a 3D cardiac model representative of a heart of the patient as a function of at least an ultrasound image wherein the at least an ultrasound image includes a two-dimensional image of the heart of the patient and wherein the 3D cardiac model includes a three dimensional interpolation of the two-dimensional image, determine a valve model datum as a function of the 3D cardiac model, receive at least valve model representative of at least a cardiovascular device to be placed within the patient as a function of the valve model datum and display the at least a 3D cardiac model and at least a valve model.
Resumen de: WO2026075575A1
The current invention relates to electroconductive bioinks, as well as their method of obtaining and their use in food production. The described electroconductive bioinks feature a high capability for cell support, as well as excellent printability and high organoleptic and nutritional properties. The present invention also relates to a method of obtaining a food product through bioprinting by 3D extrusion of the electroconductive bioinks and of the resulting food product. The invention represents as an alternative to food production by 3D extrusion bioprinting associated to cellular agriculture techniques.
Resumen de: WO2026074268A2
The invention relates to a device comprising an expandable hollow hydrogel tube encapsulated by an ingestible capsule to enable the targeted delivery of large molecules such as biologics to the gastrointestinal (GI) mucosa. Upon ingestion, the capsule is arranged to release the hydrogel tube in the GI tract, where the hydrogel tube expands from a first configuration to a second configuration upon hydration. In its expanded state, the hydrogel tube exerts an outward radial force on the lining of the GI tract. In some embodiments, the outward-facing surface of the hydrogel tube comprises microneedles. The invention further relates to a hydrogel resin comprising: gelatin or poloxamer 407; a neutralisation agent; acrylic acid or sodium acrylate; a crosslinker; a photoinitiator; and a photoabsorber. The hydrogel tube of the invention may be produced by bioprinting and photo-crosslinking said hydrogel resin.
Resumen de: US20260100274A1
A system for configuring medical devices in a healthcare facility. The system receives a selection to configure one or more medical devices and generates a first electronic document that includes editable inputs for modifying one or more settings on the one or more medical devices. The system exports the first electronic document and receives one or more edits for modifying the one or more settings of the one or more medical devices and a signature. The system generates a second electronic document based on the one or more edits and exports the second electronic document for modifying the one or more settings of the one or more medical devices.
Resumen de: WO2026074549A1
This invention, titled "Medical Identification and Signal Tag System", addresses the growing challenge of maintaining accurate and timely patient monitoring in high-stress clinical environments such as emergency rooms and operating theaters. The technical problem targeted by this invention stems from the overwhelming workload, fragmented patient data systems, and delayed response times that often lead to medical errors and professional burnout among healthcare workers. To overcome these limitations, the invention integrates an Advanced Monitoring Analytics Module with a Wearable Medical Identification Tag. The system automatically analyzes patients' vital signs using artificial intelligence and machine learning algorithms capable of detecting critical physiological changes in real time. These algorithms dynamically interpret multi-parameter inputs such as heart rate, blood pressure, oxygen saturation, and body temperature and issue immediate alerts to the medical staff through a secure wireless connection. Technically, the invention employs a dual-component architecture. The monitoring unit, attached to the hospital's existing patient monitor, collects and processes biosignals using a high-speed microcontroller and a neural processing unit (NPU). The second component, the wearable tag, communicates via BLE protocol and provides visual, vibrational, and digital alerts through LED indicators and an integrated LCD interface. A secure encryption layer ensures data confidentiality
Resumen de: US20260096783A1
0000 An apparatus and method for subject monitoring and diagnosing with non-invasive measures are disclosed. The apparatus includes a memory contains instructions configuring at least a processor to generate invasive measurement training data, train an invasive measurement machine-learning model using the invasive measurement training data, receive non-invasive measurement data, wherein the non-invasive measurement data includes electrocardiogram (ECG) data and echocardiogram (echo) data and the non-invasive measurement data includes information that is obtained through non-invasive measurements, fuse the ECG data and the echo data into a fused non-invasive measurement datum, generate at least an invasive measurement datum as a function of the fused non-invasive measurement datum using the trained invasive measurement machine-learning model, wherein the at least an invasive measurement datum includes information that can be obtained through invasive measurements and transmitting the at least an invasive measurement datum to a remote device.
Resumen de: US20260096731A1
0000 Systems and methods for biometric analysis are described. In some embodiments, a system may include a wearable device configured to be worn on a portion of an arm of a user while the user sleeps. The wearable device may include a plurality of electrodes disposed on an interior of the wearable device and configured to obtain biopotential signals from the user's arm. The system also may include a processor configured to analyze biopotential data derived from the biopotential signals to determine one or more characteristics relating to sleep of the user, and generate an output based on the one or more characteristics relating to the sleep of the user.
Resumen de: US20260098923A1
The disclosure relates to devices and methods for applying a magnetic field on a body of a patient. The time-varying magnetic field may applied to a brain of the patient. The disclosure provides a method of finding the position suitable for application of the magnetic field to the brain. The devices and methods of the disclosure may be suitable for reducing of food craving.
Resumen de: US20260096780A1
0000 In accordance with a method of detecting a pressure induced sensor artifact (PISA) in an analyte trace, a measured analyte trace having a plurality of data samples obtained over a period of time from an analyte sensor is received. A reconstructed analyte trace and an associated confidence window is generated from the measured analyte trace using a Bayesian denoising algorithm that includes a model that models the measured analyte trace as a sum of an unknown true analyte trace and a measurement error. The measured analyte trace is compared to the reconstructed analyte trace to identify data samples in the measured analyte trace that are located outside of the confidence window as being associated with a PISA.
Resumen de: US20260097234A1
Presented herein are systems and methods for generating data structures for data structures for events detected across data sources in network environments. A computing system may maintain, on a data repository, a profile for a subject at risk of or diagnosed with cancer.The profile may identify a plurality of event identifiers for a corresponding plurality of events associated with administration of radiotherapy to the subject. The computing system may apply a prompt based on a request and at least a portion of the profile to a generative machine learning (ML) model. The computing system may generate, based on applying the prompt to the generative ML model, a data structure comprising (i) a plurality of nodes corresponding to the respective plurality of event identifiers and (ii) a plurality of edges each defining a relationship between a corresponding pair of the plurality of nodes.
Resumen de: WO2026076473A1
The disclosed bracket comprises a customized pad with an offset-defined envelope surface and a plurality of retentive features. These retentive features may include protrusions, depressions, or discrete discontinuous structures, while fracture features and removal features are incorporated to facilitate controlled debonding. Such structural designs enhance adhesive contact, improve bonding strength, and enable easier, safer bracket removal at the end of orthodontic treatment.
Resumen de: US20260096910A1
0000 A prosthetic assembly includes a socket and a liner. The socket includes a first interlocking feature and defines an inner volume. The liner includes a second interlocking feature. The first interlocking feature and the second interlocking feature are configured to engage each other when the liner is inserted into the inner volume of the socket. The liner is configured to receive a distal limb of a patient. At least one of the socket or the liner include inner voids extending within walls of the socket or the liner.
Resumen de: CN119863574A
The invention relates to the technical field of three-dimensional reconstruction, and provides a three-dimensional reconstruction method and device, electronic equipment and a storage medium, and the method comprises the steps: obtaining a first image frame set of an oral cavity in a first state, and the oral cavity in the first state represents that at least one actual scanning rod is installed in the oral cavity; identifying a scanning rod area of each image frame in the first image frame set; and based on the feature information in the scanning rod region, splicing the plurality of image frames in the first image frame set, and reconstructing to obtain target three-dimensional data corresponding to an actual scanning rod in the oral cavity. According to the method, splicing is carried out based on the rigid structure, the influence of anatomical structures (such as gingiva, lip and tongue) in the image frame on the splicing precision can be reduced, and the overall precision of three-dimensional reconstruction can be improved.
Resumen de: US20260097192A1
An electronic device according to an example may comprises: a cartridge accommodation part for accommodating a cartridge including emulsion therein; a crushing circuit including a crushing element capable of crushing at least a portion of the cartridge arranged in the cartridge accommodating part; a processor for generating a crushing signal; a transfer circuit for transferring the crushing signal to the crushing circuit; and a microneedle for discharging, to the outside of the electronic device, the emulsion exposed by the crush of at least a portion of the cartridge.
Nº publicación: KR20260047964A 09/04/2026
Solicitante:
주식회사엘지생활건강
Resumen de: KR20260047964A
0001a 본 개시의 실시예에 의하면, 프린터용 클리닝 장치, 이를 포함하는 휴대용 프린터 어셈블리, 및 휴대용 프린터의 클리닝 방법이 제공된다. 상기 프린터용 클리닝 장치는, 제1 베이스 면 및 제2 베이스 면을 포함하는 클리닝 보디 및 상기 클리닝 보디의 적어도 일부에 형성된 클리닝 개구부를 포함하는 클리닝 베이스부; 상기 클리닝 보디의 상기 제1 베이스 면 상에 이동 가능하도록 결합될 수 있으며, 가이드 개구부를 포함하는 클리닝 가이드부; 및 클리닝 부재와 결합된 상태에서 상기 클리닝 개구부에 배치되어 상기 클리닝 베이스부와 결합될 수 있는 클리닝 툴; 을 포함할 수 있다. 상기 클리닝 툴이 상기 클리닝 베이스부에 결합되는 경우, 상기 클리닝 부재는 제1 베이스 면 상에서 노출될 수 있다.