5183 results about "Medical equipment" patented technology

A system for transferring data into and out of medical devices wherein a personal data manager (PDM) is used in a web-based network is disclosed. The PDM co-operates with a programmer to enhance remote monitoring of implanted medical devices on a chronic basis to deliver clinical therapy in real time. The PDM is handheldable and mobile and expands the reach of the programmer by storing and forwarding data from the programmer to web-based network constituting a medical environment. The PDM is also implemented to store and forward information to PCs and similar peripheral equipment. In a specialized application, the PDM is configured to exchange data with the unregulated operational/functional segments of the IMD.

A portable patient communicator (PPC) includes a portable housing that supports a processor coupled to memory for storing medical firmware and wireless radio firmware, first and second radios, a processor, and a power source. Communications between a patient implantable medical device (PIMD) and the first radio of the PPC are effected in accordance with program instructions of the medical firmware, and communications between the second radio of the PPC and the wireless network are effected in accordance with program instructions of the wireless radio firmware. Data from the PIMD is received via the first radio to which a priority level is assigned, such as in a tiered manner. A data transport mechanism is selected among disparate data transport mechanisms based at least in part on the priority level. PIMD data is transmitted to the wireless network using the selected transport mechanism via the second radio.

Disclosed herein are systems and methods for syndication and management of structured and unstructured data to assist institutional healthcare delivery, healthcare providers' practices, healthcare providers' group practices, collaborative academic research and decision making in healthcare, including through the utilization of medical devices and healthcare pools.

A system and method for identifying, locating, and managing inventory of sterilized medical devices located within a sealed sterilization case in preparation for a surgical procedure. Communication tags, such as radio frequency identification (RFID) and/or Global Positioning System (GPS) tags, are connected to the medical device and communicate information wirelessly. Information is obtained from the communication tags and sent to the database where it is compared with the information in the database. The results may be displayed on the interface thereby providing the user with information about the medical instruments contained in the sealed sterilization case without breaking the seal of the sealed sterilization case.

A system apparatus and method of monitoring in a secured fashion the access, storage and retrieval of information, using a networked modular wireless device. The system may include a network of wireless, Wi-Fi devices (or any other wireless communication mechanism such as GPRS, GSM, iDen), or Nodes, each one of them possibly controlling the access to a medically sensitive object, such as a drawer (or cabinet) or to a medical device, or to another information source, item of equipment, drug, etc as well as tracking via RFid readers the access to the records or information contained in it. In the case of a physical file, each file has an RFid tag on it that is being read when removed or returned to the cabinet. Access to the cabinet and physical records, or to the medical device is monitored by reading the RFiD identity card of personnel accessing the cabinet or medical devices. In addition to controlling the access to the cabinet or medical device by controlling the cabinet lock (or in the case of a small medical device, the lock of an IV, injection device, specimen collection unit, or of a large medical device such as a defibrillator), the node can alert electronically by sending a message to the controlling unit, or by sending a physical alert (such as an alarm signal), when unauthorized personnel is attempting to access the cabinet, the files or devices. The system is useful in the context of monitoring the information contained in physical files, such as medical information, and can be used for access to medical devices, in order to better monitor the authorization rights of personnel participating in processes such as drug delivery or specimen collection. A control unit monitors activity at a plurality of nodes, and assists in storing the list of authorized personnel and files, and can store electronically captured information regarding the physical files (for example, the reason for accessing the file and reasons for changes in it) or medical device. The system can communicate with other information management systems.

A system for the collection, management, and dissemination of information relating at least to a medical procedure is disclosed. The system includes a user interface adapted to provide raw data information at least about one of a patient, the medical procedure, and a result of the medical procedure. A medical device communicates with the user interface, receives the raw data information from the user interface, and generates operational information during use. A central database communicates at least with the medical device and receives data from the medical device. The central database is used to create related entries based on the raw data information and the operational information and optionally transmits the related entry to the medical device or the medical device user. The related entry includes information that provides guidance based on previously tabulated, related medical procedures. A system for the iterative analysis of medical standards is also disclosed along with methods for the evaluation of medical procedures and standards.

The present invention provides systems and methods for supporting encrypted communications with a medical device, such as an implantable device, through a relay device to a remote server, and may employ cloud computing technologies. An implantable medical device is generally constrained to employ a low power transceiver, which supports short distance digital communications. A relay device, such as a smartphone or WiFi access point, acts as a conduit for the communications to the internet or other network, which need not be private or secure. The medical device supports encrypted secure communications, such as a virtual private network technology. The medical device negotiates a secure channel through a smartphone or router, for example, which provides application support for the communication, but may be isolated from the content.

A medical practice management system of the present invention acquires schedule information on a medical practice to be administered to a patient. Information on medical equipment corresponding to the acquired schedule information is selected from among pieces of information on medical equipment to be used in medical practices, stored in association with a plurality of pieces of schedule information, respectively. Then, the acquired schedule information and the selected information on medical equipment are managed in association with each other.

Disclosed herein are systems and methods for syndication and management of structured and unstructured data to assist institutional healthcare delivery, healthcare providers' practices, healthcare providers' group practices, collaborative academic research and decision making in healthcare, including through the utilization of medical devices and healthcare pools.

There is provided a modular polyaxial pedicle screw assembly that includes various components which may be configured in various manners so as to provide different functionalities to the pedicle screw assembly. This advantageously decreases surgery time, reduces repetitive and tedious surgical steps, and allows for streamlining inventory of expensive medical equipment. In one embodiment, a pedicle screw assembly includes a pedicle screw, a rod holding element, a polyaxial insert, a rod, and a set screw. The pedicle screw includes a threaded shaft and a cap. The rod holding element includes a screw hole, an insert bearing area, a chamber, chamber walls, a saddle area, and a threading area. The insert is disposed within the chamber, and the insert defines a bearing surface, an upper surface, side walls and a receiving area. The insert is positioned within the chamber such that the insert bearing surface contacts the rod holding element insert bearing area; additionally the side walls of the insert can bear against the chamber walls. The pedicle screw is positioned so that the screw shaft passes through the screw hole of the rod holding element and the screw cap rests within the receiving area of the insert. The rod is disposed so as to rest on the upper surface of the insert; and the set screw, joined to the threading area of the rod holding element, secures the rod to the upper surface of the insert.

The determination of analyte concentration in physiological samples is of ever increasing importance to today's society. Such assays find use in a variety of applications, including clinical laboratory testing, home testing, etc., where the results of such testing play a prominent role in the diagnosis and management of a variety of disease conditions. An apparatus is described herein which may be used for the manufacture of medical devices which include an integrated lancet and sensor.

The invention addresses hardware and software products capable to make contemporaneous accurate predictions regarding how a person's biological system will respond to a serious of stimuli. The predictions can then be communicated in real time, enabling confirmation of good control status, need for corrective action, planning future actions, or even outside intervention in case of emergency. Also addressed by the invention is a family of diagnostic hardware based on intelligent optoelectronic sensors that incorporate one or more Wedge-and-Strip Position-Sensitive Photo-Detectors optimized for probabilistic real time evaluation of spectroscopy data from living subjects.

One method according to the present invention includes receiving data wirelessly from a plurality of medical devices, transmitting the data to an intermediary device (such as a properly equipped mobile telephone or personal digital assistant), and formatting a message including the received data for transmission to a medical data server. This method can be practiced automatically to allow a medical device for a patient or other subject to be monitored without requiring the patient to manually enter information. This method also allows for multiple different medical devices to be monitored, even where such devices each communicate on different frequencies and/or using different communication protocols.

A system according to one aspect of the present invention comprises a processor, a plurality of medical device transceivers, a data relay transceiver, and a memory coupled to the processor, and storing instructions. Each medical data transceiver is configured to receive data wirelessly from one or more medical devices. The processor executes the instructions in the memory to receive data from one or more medical devices using the plurality of medical device transceivers (which gathers data concerning the patient's condition), and transmits the data to an intermediary device using the data relay transceiver. This system can be implemented in a small, portable unit that is easy for a patient to transport. The system can communicate with multiple medical devices, regardless of the frequency or communications protocol utilized by each of the medical devices, and can retransmit (and optionally reformat) data from the medical device(s) to any desired recipient using any suitable frequency(ies) and communication protocol(s).

The invention discloses a lower limb exoskeleton rehabilitation robot in the technical field of medical equipment. The lower limb exoskeleton rehabilitation robot comprises an ankle joint motion module, a knee joint motion module, a hip joint motion module, a hip and support module and a crutch module, wherein one end of the knee joint motion module is connected with the ankle joint motion module, and the other end of the knee joint motion module is connected with the hip joint motion module; the hip and support module is connected with the hip joint motion module; and the crutch module is independent of an exoskeleton body. The lower limb exoskeleton rehabilitation robot can help patients who suffer from paraplegia stand up and walk, and the bend and stretch motion of a knee joint and a hip joint is controlled by collecting contact information of a crutch and the ground so as to help the patients to stride; and an oppositely-pulled spring of the knee joint can help to reduce impact from the ground, so that patients can walk comfortably, and the efficiency of rehabilitation training is improved.

The invention relates to an apparatus for self-treatment of diabetes. The apparatus is particularly advantageous by comprising a plurality of devices each of which has its own dedicated function corresponding to a number of acts which a diabetic must perform on himself. The individual devices are mutually interconnectible, and the combination comprises at least a body fluid analyser and a dosing apparatus for administering a predetermined dose of insulin to the patient. Each of the devices may be provided in several sizes so that the user himself may combine the relevant devices of the relevant size with respect to the current need. This reduces the risk of forgetting parts of the equipment, and the confidence of using the equipment is enhanced because it is evident to the user that it is a complete apparatus consisting of unified parts.

A medical equipment control system consists mainly of a plurality of centralized controllers each of which controls on a centralized basis a plurality of pieces of medical equipment installed in an operating room, and a mobile device capable of communicating with the plurality of centralized controllers. The mobile device is used to determine or record control data based on which the plurality of pieces of medical equipment is controlled. The recorded control data is transmitted to and recorded in the centralized controller in an operating room concerned. Thus, a medical equipment control system capable of controlling medical equipment at low cost on a centralized basis is realized.

Systems and methods for measuring, collecting, managing, reporting and distributing data pertaining to medical device measurements, such as personal health condition data, are provided. In various embodiments, medical device(s) are paired (integrated, tethered, or wirelessly coupled) with a user's portable computing device, such as a cell phone, so that the portable device receives locally made health data measurement(s) recorded by the medical device(s). After any pre-processing by the portable device, standard interfaces enable the health data measurement(s) to be transmitted, e.g., periodically, from the portable device to a health station server on a wireless communications network. The health station server may then analyze the health data measurement(s), e.g., versus historical and demographic data, so that the results of the analysis can be distributed to end users and service providers alike who make use of the communications network in a variety of ways.

A system integrates diagnostic, therapeutic, monitoring and other devices commonly found in a healthcare environment into a Hospital Information System (HIS) to improve the delivery of healthcare. The system uses intelligent, networked diagnostic, therapeutic, monitoring and other devices to provide device performance and availability information. A medical device management system includes a repository of patient medical records and a scheduling system for use in scheduling of a medical procedure for a particular patient. A configuration manager in bidirectional communication with a medical device automatically initiates pre-configuration of the medical device for use in the medical procedure using medical record information of the particular patient derived from the repository, in response to scheduling of the particular patient to receive the medical procedure.

The present invention provides for the electrochemical generation of ozone for use in "point-of-use" applications. The electrochemical ozone generators or systems of the present invention may be used to provide disinfected water, ozone-containing water, and/or ozone gas. Disinfected water may be produced by introducing ozone gas into a potable or purified water source for the purpose of disinfecting or controlling the microorganisms in the water source. Ozonated water or ozone gas may be produced and provided for various anti-microbial and cleansing applications of the consumer, such as washing food, clothing, dishes, countertops, toys, sinks, bathroom surfaces, and the like. Furthermore, the ozone generator may be used to deliver a stream of ozone-containing water for the purpose of commercial or residential point-of-use washing, disinfecting, and sterilizing medical instruments and medical equipment. For example, the ozone-containing water may be used directly or used as a concentrated sterilant for the washing, disinfecting, and sterilizing of medical instruments or equipment. Ozone gas may also be used in many of the foregoing examples, as well as in the deodorization of air or various other applications. The invention allows the electrochemical ozone generator to operate in a nearly or entirely passive manner with simplicity of design.

Methods, systems, and apparatus for detecting an epileptic event, for example, a seizure in a patient using a medical device. The determination is performed by providing an autonomic signal indicative of the patient's autonomic activity; providing a neurologic signal indicative of the patient's neurological activity; and detecting an epileptic event based upon the autonomic signal and the neurologic signal.

Embodiments of the present invention provide devices and methods that allow a continuous connection to be maintained between a medical device that is capable of communicating over a cellular network and a sensor network. Medical devices that are capable of communicating over a cellular network represent one form of assistive technologies for the home that can allow senior citizens to remain at home for longer, improve the quality of life, and provide more cost-effective solutions than residential care. Removing a SIM card (subscriber identity module, a removable smart card for cell phones that securely stores the service-subscriber key used to identify a mobile phone) from a cellular communication device requires the device to be powered down. However, powering down a medical device can result in a loss of important data.

A heating assembly, including a blanket portion and a control apparatus for electrically heating the blanket portion. The control apparatus generates direct current power of desired wave form to enable the assembly to be used for warming patients without interference of medical equipment as may be used in the process of a surgery. Alternate power sources include battery power and alternating current power transformed by a transformer into direct current power.

A medicine dispensing system is provided that comprises of a medicine container with an inbuilt pill dispensing assembly which automatically dispenses a prescribed dose of medicine at prescribed times. It alerts the patient when a dose of medicine has been dispensed. The alert signal is a local audio or visual alarm or a remote reminder by phone, wireless network or internet. A modem and communication ports are provided which enable the said medicine container to communicate with remote parties like health care professionals and medical devices such as glucose meter. This feature allows remote medicine management, disease management and health education. An internal microprocessor and a memory chip control and execute electronic functions of the said medicine container. Sensors are provided to detect whether a dose has been dispensed and whether it is consumed. The said medicine container is able to record, analyze and report patient's compliance with a medicine regimen.

The invention relates to a noninvasive radiotherapy system for a robot, and belongs to the medical equipment field. The noninvasive radiotherapy system for the robot consists of seven modules, i.e. a radiotherapy planning system, a three-dimensional numerical-control therapy bed, an automatic tracking system for a four-dimensional real-time image, a robot system, a radioactive source, an adjuvant therapy system and an integrated control system, wherein the automatic tracking system for the four-dimensional real-time image consists of a six-freedom-of-degree G-shaped arm real-time image system and an intelligent tracking system; the six-freedom-of-degree G-shaped arm real-time image system is formed by successively connecting a G-shaped arm, a G-shaped arm sliding rail, a G-shaped arm spindle, a G-shaped arm pitch shaft and a G-shaped arm sliding seat; an X ray source and an X ray dynamic flat panel detector are formed into one group, and two groups are correspondingly installed on the G-shaped arm; and the G-shaped arm sliding seat is installed in a rail (9). According to the noninvasive radiotherapy system for the robot, which is disclosed by the invention, the defects of unmatched projection time, time waste and low therapy precision in the prior art are overcome, the precise therapy of the whole body tumor can be carried out, and the cardiovascular disease therapy and the noninvasive regulation of the renal nerve disease can be carried out.

A reporting system, including a processing device, and method provides drug and medical device safety and support information during a workflow of a healthcare provider. The system and method electronically acquires, maps, generates, compiles, verifies and transfers in real time critical information regarding particular drugs and medical devices required by healthcare providers, such as a prescriber, at the optimum time in which the healthcare provider needs the information. In an embodiment, the drug and medical device safety information is accessed from an associated healthcare website, such as an Electronic Health Record (EHR) web site, during a prescription stage in the healthcare providers workflow for a particular patient. The system and method also includes an adverse reporting system that allows for the drug and medical device safety information to be updated and accurately reported in an efficient and up to date manner. In an embodiment, a healthcare provider reports an adverse event or reaction to a drug by a patient during a workflow at a EHR web site. The adverse event information is forwarded to the Federal Drug Administration (FDA) and the particular drug manufacturer which may update the corresponding drug information. The updated drug information may then be reported by the system to insure that healthcare providers receive the most current, accurate and complete safety information during a workflow. In embodiments, the updated drug and medical information may be provided to malpractice insurance carriers to further ensure safety.

The invention relates to the technical field of medical equipment, and in particular relates to an automatic control transfusion device and an automatic control method thereof. The automatic control transfusion device comprises a transfusion system and an automatic control system, wherein the transfusion system comprises a hanging support, transfusion bags and a transfusion apparatus; and the automatic control system comprises a force sensor, an on-off control device and a control unit. The method comprises the following steps of: detecting weights of the transfusion bags, calculating the liquid remaining quantity according to the weights of the transfusion bags, cutting off a transfusion pipeline and giving an alarm when the liquid remaining quantity is less than a threshold value. The automatic control transfusion device and the automatic control method thereof, disclosed by the invention, have the advantages that: the alarm can be given early and the transfusion pipeline can be automatically cut off when the liquid is going to drip off; the automatic switchover between the transfusion bags can be controlled; manual operation of medical workers is not needed; and the alarm adopts a plurality of types such as sound, light and the like, different alarm sounds and lights can be set according to different situations, the reliability is strong and the transfusion safety can be fully guaranteed.

Methods for analyzing, evaluating, and controlling risk of errors in language translation of medical device labeling are disclosed. The disclosed methods include identifying the risk level of the device; identifying the safety function(s) of the content that is translated; evaluating risks associated with the translation process; and analyzing this risk information and applying it in the selection of resources and in the design and execution of processes, to effectively mitigate the risk of safety related translation errors in labeling for medical devices.

The invention provides, in some aspects, medical apparatus with software-based cursor control and graphical user interface hotspot selection. This can be used, by way of non-limiting example, as part of a graphical user interface by which doctors, nurses, patient care technicians, other health care providers, and/or patients can enter data into enter data and/or to control the apparatus and/or associated medical equipment.

There is provided a modular pedicle screw assembly that includes various components which may be configured in various manners so as to provide different functionalities to the pedicle screw assembly. This advantageously decreases surgery time, reduces repetitive and tedious surgical steps, and allows for streamlining inventory of expensive medical equipment. In one embodiment, a pedicle screw assembly includes a pedicle screw, a rod holding element, an insert, a rod, and a set screw. The pedicle screw includes a threaded shaft and a cap. The rod holding element includes a screw hole, an insert bearing area, a chamber, chamber walls, a saddle area, and a threading area. The insert is disposed within the chamber, and the insert defines a bearing surface, an upper surface, side walls and a receiving area. The insert is positioned within the chamber such that the insert bearing surface contacts the rod holding element insert bearing area; additionally the side walls of the insert can bear against the chamber walls. The pedicle screw is positioned so that the screw shaft passes through the screw hold of the rod holding element and the screw cap rests within the receiving area of the insert. The rod is disposed so as to rest on the upper surface of the insert; and the set screw, joined to the threading area of the rod holding element, secures the rod to the upper surface of the insert. The insert may have a uniplanar configuration which allows movement of the insert, prior to final attachment, in a plane of motion. The insert may optionally have a monoaxial configuration which prevents movement of the insert.