A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s pressure threshold and pain tolerance. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A hand-held, non-powered mechanical device intended to be used by a healthcare p
A hand-held, non-powered mechanical device intended to be used by a healthcare professional for the adjustment, mobilization, or manipulation of the joints of the spine and/or extremities. This is a reusable, non-invasive, non-surgical, non-sterile, transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A hand-held, non-powered mechanical device intended to be used by a healthcare p
A hand-held, non-powered mechanical device intended to be used by a healthcare professional for the adjustment, mobilization, or manipulation of the joints of the spine and/or extremities. This is a reusable, non-invasive, non-surgical, non-sterile, transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A hand-held, non-powered mechanical device intended to be used by a healthcare p
A hand-held, non-powered mechanical device intended to be used by a healthcare professional for the adjustment, mobilization, or manipulation of the joints of the spine and/or extremities. This is a reusable, non-invasive, non-surgical, non-sterile, transient device.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s pressure threshold and pain tolerance. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
For the wireless mode version of the subject device, combined with an applicatio
For the wireless mode version of the subject device, combined with an application installed on a tablet that can be used in a home environment, the content of the SPM01K4 convenience kit is: 1 electrostimulator SPM01M1 configuration; electrodes; protective skin, and 1 tablet with the MySPM@Home mobile application (SPM01A2).
For the wireless mode version of the subject device, to be used in combination w
For the wireless mode version of the subject device, to be used in combination with an application installed on a tablet, the SPM01K3 convenience kit includes: 1 electrostimulator SPM01M1 configuration; electrodes; protective skin, and 1 tablet with the MySPM mobile application (SPM01A1).
For the wireless mode version of the subject device, to be used in combination w
For the wireless mode version of the subject device, to be used in combination with a dedicated control software running on a pc/laptop, the content of the SPM01K2 convenience kit is: 1 electrostimulator SPM01M2 configuration; electrodes, and protective skin.
For the stand-alone mode version of the subject device, the SPM01K1 convenience
For the stand-alone mode version of the subject device, the SPM01K1 convenience kit includes: 1 electrostimulator SPM01M1 configuration; electrodes, and protective skin.
Optionally, the electrostimulator (SPM01M1) can require the combined use with th
Optionally, the electrostimulator (SPM01M1) can require the combined use with the MySPM@Home mobile application, as accessory of the Subject device. It allows to monitor the user and guide rehabilitation and training through specific protocols.
Optionally, the electrostimulator (SPM01M1) can require the combined use with th
Optionally, the electrostimulator (SPM01M1) can require the combined use with the MySPM mobile application, as accessory of the Subject device. It allows to monitor the user and guide rehabilitation and training through specific protocols.
The configuration is composed of an electrostimulator and other components, usef
The configuration is composed of an electrostimulator and other components, useful for recharging, wearing, stimulating and/or controlling it. The SPM01M2 configuration supports IEEE 802.15.4 radio interface. In this case it provides for the exchange of data between the stimulator and a receiver connected to the PC, which then collects the data sent by the device and synchronizes the transmission. The dedicated control software is supplied via an usb receiver.
The configuration is composed of an electrostimulator and other components, usef
The configuration is composed of an electrostimulator and other components, useful for recharging, wearing, stimulating and/or controlling it.The SPM01M1 configuration supports Bluetooth Low Energy communication. In this case it can connect directly to a smartphone/tablet on which a dedicated app is installed. The dedicated control software is supplied via an usb receiver and must be used by a properly trained healthcare professional.
Accurate measurements of upper and lower extremity ROM with precise electronic t
Accurate measurements of upper and lower extremity ROM with precise electronic tools for evaluation and progress reporting:Wrist, Forearm, Elbow, Shoulder, Hip, Knee, Ankle, Documentation of amputation, ankylosis, and arthrodesis for the above jointsThis product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13
Accurate measurements of upper and lower extremity ROM with precise electronic t
Accurate measurements of upper and lower extremity ROM with precise electronic tools for evaluation and progress reporting.Hand (fingers and thumb) – active and passive, extension and flexion, abduction and adduction, lateral deviations and rotational deformities, calculation of total active motion and total passive motionWrist – active and passive, extension and flexion, radial and ulnar deviationThis product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13
A modern microprocessor controlled general purpose amplifier system which is des
A modern microprocessor controlled general purpose amplifier system which is designed to be worn by the subject. The Amplifier (K800) provides a user friendly method for collecting signals from a variety of sensors including goniometers, sEMG and related signals, in a format which may readily be connected to proprietary display and recording systems including A/D cards.This product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13
DataLINK (DLK900) is an on-line general purpose subject worn programmable Data A
DataLINK (DLK900) is an on-line general purpose subject worn programmable Data Acquisition System allowing the user to collect both analog and digital data from a wide range of wired sensors including Biometrics' Goniometers, Torsiometers, active EMG sensors, Accelerometers, Pinchmeters, Hand Dynamometers and Contact Switches.This product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13.
The Biometrics Analysis Software is a comprehensive tool for EMG, Goniometer and
The Biometrics Analysis Software is a comprehensive tool for EMG, Goniometer and associated sensor analysis including real-time data analysis as the data is collected. The Analysis software also contains all of the features of the Management Software: The DataLINK Management Software allows the user to set up the DataLINK communications with the computer, configure the sensors, collect and save the data. the Management software also contains the Dynamic Link Library for streaming dataSoftware is available in English, Chinese, and Japanese.
The DataLINK Management Software allows the user to set up the DataLINK communic
The DataLINK Management Software allows the user to set up the DataLINK communications with the computer, configure the sensors, collect and save the data. the Management software also contains the Dynamic Link Library for streaming data to third party software.Software is available in English, Chinese, and Japanese.
DataLINK (DLK900) is an on-line general purpose subject worn programmable Data A
DataLINK (DLK900) is an on-line general purpose subject worn programmable Data Acquisition System allowing the user to collect both analog and digital data from a wide range of wired sensors including Biometrics' Goniometers, Torsiometers, active EMG sensors, Accelerometers, Pinchmeters, Hand Dynamometers and Contact Switches.This product is independently tested and certified to BS EN 60601-1:2006 + A1:2013
The DataLOG is the latest in data acquisition technology developed to meet the n
The DataLOG is the latest in data acquisition technology developed to meet the needs of researchers for portable data collection and monitoring in human performance, sports science, medical research, industrial ergonomics, gait laboratories, and educational settings. Includes: 8 channel data acquisition unit, Bluetooth adapter, 6 x Micro SD cards, Card reader, Management Software, instrument caseThis product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13
The Biometrics Analysis Software is a comprehensive tool for EMG, Goniometer and
The Biometrics Analysis Software is a comprehensive tool for EMG, Goniometer and associated sensor analysis including real-time data analysis as the data is collected. The Analysis software also contains all of the features of the Management Software: The DataLOG Management Software allows the user to set up the DataLOG communications with the computer, configure the sensors, collect and save the data. the Management software also contains the Dynamic Link Library for streaming dataSoftware is available in English, Chinese, and Japanese.
The DataLOG Management Software allows the user to set up the DataLOG communicat
The DataLOG Management Software allows the user to set up the DataLOG communications with the computer, configure the sensors, collect and save the data. the Management software also contains the Dynamic Link Library for streaming data to third party software.Software is available in English, Chinese, and Japanese.
The DataLOG is the latest in data acquisition technology developed to meet the n
The DataLOG is the latest in data acquisition technology developed to meet the needs of researchers for portable data collection and monitoring in human performance, sports science, medical research, industrial ergonomics, gait laboratories, and educational settings. Includes: 8 channel data acquisition unit, Bluetooth adapter, 6 x Micro SD cards, Card reader, Management Software, instrument caseThis product is independently tested and certified to BS EN 60601-1:2006 + A1:2013
The Biometrics Analysis Software is a comprehensive tool for EMG, Goniometer and
The Biometrics Analysis Software is a comprehensive tool for EMG, Goniometer and associated sensor analysis including real-time data analysis as the data is collected. The Analysis software also contains all of the features of the Management Software: The DataLITE Management Software allows the user to set up the DataLITE communications with the computer, configure the DataLITE sensors, collect and save the data. the Management software also contains the Dynamic Link Library for streaming dataSoftware is available in English, Chinese, and Japanese.
The DataLITE Management Software allows the user to set up the DataLITE communic
The DataLITE Management Software allows the user to set up the DataLITE communications with the computer, configure the DataLITE sensors, collect and save the data. the Management software also contains the Dynamic Link Library for streaming data to third party software.Software is available in English, Chinese, and Japanese.
Mains powered battery charging unit for up to 8 wireless DataLITE sensors (LE230
Mains powered battery charging unit for up to 8 wireless DataLITE sensors (LE230, W series Goniometers, Z series Torsiometers, AD2, ACL500).Includes Medical Grade Power Supply and country specific mains power cord..This product is independently tested and certified to BS EN 60601-1:2006 + A1:2013
A small wireless Dongle (receiver) attached to the USB port of the host PC (Wind
A small wireless Dongle (receiver) attached to the USB port of the host PC (Windows 8 or 10 compatible) can communicate with up to 24 channels of DataLITE sensor inputs via Wi-Fi. When used with a Windows 10 Tablet, the researcher can monitor and analyse data in real-time while the subject has total freedom of movement in laboratory or field studies.This product is independently tested and certified to BS EN 60601-1:2006 + A1:2013
Accurate measurements of upper and lower extremity ROM with precise electronic t
Accurate measurements of upper and lower extremity ROM with precise electronic tools for evaluation and progress reporting.The Biometrics Range of Motion Kit (R500) provides precise electronic tools for:upper and lower extremity range of motion measurements
Accurate measurements of upper and lower extremity ROM with precise electronic t
Accurate measurements of upper and lower extremity ROM with precise electronic tools for evaluation and progress reporting:Wrist, Forearm, Elbow, Shoulder, Hip, Knee, Ankle, Documentation of amputation, ankylosis, and arthrodesis for the above jointsThis product is independently tested and certified to BS EN 60601-1:2006 + A1:2013
Accurate measurements of upper and lower extremity ROM with precise electronic t
Accurate measurements of upper and lower extremity ROM with precise electronic tools for evaluation and progress reporting.Hand (fingers and thumb) – active and passive, extension and flexion, abduction and adduction, lateral deviations and rotational deformities, calculation of total active motion and total passive motionWrist – active and passive, extension and flexion, radial and ulnar deviationThis product is independently tested and certified to BS EN 60601-1:2006 + A1:2013
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
A device to assist the clinician with establishing an objective assessment of a
A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient.
Sens is an inertial sensor to measure the range of motion and to compare the sym
Sens is an inertial sensor to measure the range of motion and to compare the symmetry between the injured limb’s amplitude andthe healthy limb.
The Radink Sensor uses a combination of a 3-axis accelerometer, a 3-axis gyrosco
The Radink Sensor uses a combination of a 3-axis accelerometer, a 3-axis gyroscope, and a 3-axis magnetometer to locate a patient's body in 3D space. It is calibrated to the patient's original position immediately prior to the surgery so any movement is tracked and the patient can be returned to the original position at any time during or after the surgery.