The non sterile Peña Muscle Stimulator Bipolar Probe (PS2P) is a 17 cm long reus
The non sterile Peña Muscle Stimulator Bipolar Probe (PS2P) is a 17 cm long reusable probe for use in the surgical treatment of high and low anorectal malformation. The probe has a 260 cm cord with two electrically shrouded banana plugs for attachment to the Peña Muscle Stimulator (PS2, sold separately). The probe tip consists of two gold plated polished wire probes, 0.8 mm diameter and separated by 1.8 mm. The wire probes function as the bipolar stimulus electrodes when the PS2P Probe is connected to the PS2 Stimulator.
(30) Per Case - Transcutaneous Nerve Stimulator/Electrical Muscle Stimulator Com
(30) Per Case - Transcutaneous Nerve Stimulator/Electrical Muscle Stimulator Combination with Timer -Ten Mode Dual Channel 4 Leads - Zipper Case Includes: device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual
(30) Per Case -Transcutaneous Nerve Stimulator - Three Mode with Timer Dual Chan
(30) Per Case -Transcutaneous Nerve Stimulator - Three Mode with Timer Dual Channel 4 Leads - Zipper Case Includes: device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual
(30) Per Case - Electrical Muscle Stimulator - Three Mode with Timer Dual Channe
(30) Per Case - Electrical Muscle Stimulator - Three Mode with Timer Dual Channel 4 Leads - Zipper Case Includes: device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual
(30) Per Case -Electric Muscle Stimulator -Three Mode Dual Channel 4 Leads -Zipp
(30) Per Case -Electric Muscle Stimulator -Three Mode Dual Channel 4 Leads -Zipper Case Includes, device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual
Use for symptomatic relief and management of chronic pain and/or as adjunctive t
Use for symptomatic relief and management of chronic pain and/or as adjunctive treatment in the management of post-surgical and posttraumatic acute pain. The device produces beat frequency of the range 1-250 Hz. The IF-4250D delivers very precise and repeatable Interferential therapy. Device is engineered by using ultra low power micro controller for precision, safety, durability and reliability. Key Features: 510(k) cleared device, Customizable program
The NeXus-10 MKII is designed for medical use, not restricted to a specific medi
The NeXus-10 MKII is designed for medical use, not restricted to a specific medical indication, for acquisition of (electro)-physiological signals (e.g. EEG, EMG or ECG). The product is intended to be used by medical/acces professionals in a laboratory setup or medical office, or to be set-up in such an environment after which the subject/patient can be sent out while signal acquisition continues on memory. The NeXus 10 MKII is not intended for use in diagnosis, nor in critical and/or life supporting applications.The NeXus 10 MKII is intended for use on humans.The NeXus 10 MKII is intended to be used with approved NeXus 10 MKII accessories only. Specifically, (active) sensors intended to measure specific physiological signals, shall be designed in accordance with the specifications of the NeXus-10 MKII and may require interpretation by user or application software.
The NeXus software is intended to provide (near) real-time biofeedback and neuro
The NeXus software is intended to provide (near) real-time biofeedback and neurofeedback in the form of information, visual and auditory signals, corresponding to the state of one or more physiological parameters, so that a patient can learn voluntary control of these parameters. The software shall be used on a personal computer (in a medical office environment) in combination with compatible signal acquisition devices and sensor accessories to perform its intended use. The software is designed for medical use, not restricted to a specific medical indication. It is intended to be used within a medical office environment by, or under supervision of, a health professional (novice user, technical knowledge, normal eyesight, possibly achieved with the aid of glasses). The software is not intended for use in a life support application nor is it intended for diagnostic purposes.
NC-C-GT:The GSR sensor provides a measure of skin resistance or skin conductance
NC-C-GT:The GSR sensor provides a measure of skin resistance or skin conductance when connected to a NeXus signal acquisition device, which is influenced by the autonomic activation of sweat glands in the skin. The sensor output is not intended to be used for vital monitoring purposes.The temperature sensor provides a signal that corresponds with (variations in) peripheral skin temperature when connected to a NeXus signal acquisition device. The sensor shall be placed on intact skin to provide a signal that is influenced by cutaneous blood flow. The sensor is not intended to determine directly or indirectly a measure of core body temperature and to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
NB-TMP:The temperature sensor provides a signal that corresponds with (variation
NB-TMP:The temperature sensor provides a signal that corresponds with (variations in) peripheral skin temperature when connected to a NeXus signal acquisition device. The sensor shall be placed on intact skin to provide a signal that is influenced by cutaneous blood flow. The sensor is not intended to determine directly or indirectly a measure of core body temperature and to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
NB-GSR:The GSR sensor provides a measure of skin resistance or skin conductance
NB-GSR:The GSR sensor provides a measure of skin resistance or skin conductance when connected to a NeXus signal acquisition device, which is influenced by the autonomic activation of sweat glands in the skin. The sensor output is not intended to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
NC-BVP-H (head module):The BVP sensor provides a photoplethysmography (PPG) sign
NC-BVP-H (head module):The BVP sensor provides a photoplethysmography (PPG) signal when connected to a NeXus signal acquisition device, that corresponds with variations in peripheral blood flow resulting from cardiovascular activity and responses, with the purpose of providing information on the cardiovascular variations such as heart rate variations and measured pulse amplitude. The sensor output is not intended to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
NC-BVP-F (finger module):The BVP sensor provides a photoplethysmography (PPG) si
NC-BVP-F (finger module):The BVP sensor provides a photoplethysmography (PPG) signal when connected to a NeXus signal acquisition device, that corresponds with variations in peripheral blood flow resulting from cardiovascular activity and responses, with the purpose of providing information on the cardiovascular variations such as heart rate variations and measured pulse amplitude. The sensor output is not intended to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
NB-BVP-H (head module):The BVP sensor provides a photoplethysmography (PPG) sign
NB-BVP-H (head module):The BVP sensor provides a photoplethysmography (PPG) signal when connected to a NeXus signal acquisition device, that corresponds with variations in peripheral blood flow resulting from cardiovascular activity and responses, with the purpose of providing information on the cardiovascular variations such as heart rate variations and measured pulse amplitude. The sensor output is not intended to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
NB-BVP-F (finger module):The BVP sensor provides a photoplethysmography (PPG) si
NB-BVP-F (finger module):The BVP sensor provides a photoplethysmography (PPG) signal when connected to a NeXus signal acquisition device, that corresponds with variations in peripheral blood flow resulting from cardiovascular activity and responses, with the purpose of providing information on the cardiovascular variations such as heart rate variations and measured pulse amplitude. The sensor output is not intended to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.
The NeXus-Q32 is intended for acquisition of (electro)-physiological signals (e.
The NeXus-Q32 is intended for acquisition of (electro)-physiological signals (e.g. EEG, surface EMG or ECG) from humans, regardless of any specific medical indication, by medical/research professionals.
The DuoMAG NL is intended to stimulate peripheral nerves for relief of chronic i
The DuoMAG NL is intended to stimulate peripheral nerves for relief of chronic intractable, post-traumatic and post-surgical pain.DuoMAG NL consists of a Magnetic stimulator DuoMAG XT-NL, stimulation coil, trolley MagCart, and LiquidCool System unit.
The PHYSIQ is a device provided with 4 handpieces by 2 electrodes each intended
The PHYSIQ is a device provided with 4 handpieces by 2 electrodes each intended to employ EMS (Electrical Muscle Stimulation) and TENS (Transcutaneous Electrical Nerve Stimulation) technologies for various medical applications.
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.
NEURODYN AUSSIE Sport transcutaneous neuromuscular stimulator is a four channel
NEURODYN AUSSIE Sport transcutaneous neuromuscular stimulator is a four channel stimulator with independent controls for current therapy used in AUSSIE CURRENT (Burst Modulated Medium Frequency).
NEUROTONUS MULTIWAVE transcutaneous neuromuscular stimulator is a four-channel s
NEUROTONUS MULTIWAVE transcutaneous neuromuscular stimulator is a four-channel stimulator with independente controls for current therapies used in: TENS (Transcutaneous Electrical Nerve Stimulation), FES (Functional Electrical Stimulation); RUSSIAN CURRENT (Burst Modulated Medium Frequency), AUSSIE CURRENT (Burst Modulated Medium Frequency), INTERFERENTIAL CURRENT (Amplitude Modulated Medium Frequency), DIRECT CURRENT/POLARIZED CURRENT or MICROCURRENT.
NEUROTONUS Compact transcutaneous neuromuscular stimulator is a two channels sti
NEUROTONUS Compact transcutaneous neuromuscular stimulator is a two channels stimulator with independent controls for current therapies used in: Tens (Transcutaneous Electrical Nerve
NEUROTONUS II transcutaneous neuromuscular stimulator is a four-channels stimula
NEUROTONUS II transcutaneous neuromuscular stimulator is a four-channels stimulator with independent controls for current therapies used in: TENS (Transcutaneous Electrical Nerve Stimulation), FES