Other products from "MEDHAB, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00850023296160 7 Size (3) Shoe insole size 3 (women 13.0 to 15.0) (men 11.0 to 12.50) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 STEPRITE
2 00850023296085 7 Size (4) Shoe insole size 4 (men 13.0 to 15.0) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 STEPRITE
3 00850023296061 7 Size (2) Shoe insole size 2 (women 11.0 to 12.5) (men 9.0 to 10.5) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 STEPRITE
4 00850023296054 7 Size (1) Shoe insole size 1 (women 9.0 to 10.5) (men 7.0 to 8.5) footbed wearable device that affords the patient the ability to perform exercise footbed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 STEPRITE
5 00850023296047 7 Size (0) Shoe insole size 0 (women 7.0 to 8.5) (men 5.0 to 6.5) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 STEPRITE
6 00850023296030 7 Size (00) Shoe insole size 00 (women 3.0 to 6.5) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 STEPRITE
7 00850023296351 7 Size (4) Shoe insole size 4 (men 13.0 to 15.0) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
8 00850023296344 7 Size (3) Shoe insole size 3 (women 13.0 to 15.0) (men 11.0 to 12.50) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
9 00850023296337 7 Size (2-3) Shoe insole size (2-3) (women 11.0 to 12.5) (men 9.0 to 10.5) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
10 00850023296320 7 Size (2) Shoe insole size 2 (women 11.0 to 12.5) (men 9.0 to 10.5) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
11 00850023296313 7 Size (12) Shoe insole size (12) (women 9.0 to 10.5) (men 7.0 to 8.5) footbed wearable device that affords the patient the ability to perform exercise footbed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
12 00850023296306 7 Size (1) Shoe insole size 1 (women 9.0 to 10.5) (men 7.0 to 8.5) footbed wearable device that affords the patient the ability to perform exercise footbed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RMP2 Rx
13 00850023296290 7 Size (01) Shoe insole size 1 (women 9.0 to 10.5) (men 7.0 to 8.5) footbed wearable device that affords the patient the ability to perform exercise footbed wearable device that affords the patient the ability to perform exercises both at home and in-clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
14 00850023296276 7 Size (0) Shoe insole size 0 (women 7.0 to 8.5) (men 5.0 to 6.5) Is a foot bed wearable device that affords the patient the ability to perform ex Is a foot bed wearable device that affords the patient the ability to perform exercises both at home and in clinic settings that also allows the provider the ability to make clinical judgments pursuant data collected from the patient via customizable rehabilitative protocols set, and amended, by the provider. IKK System, Isokinetic Testing And Evaluation 2 RPM2 Rx
15 00850023296023 Version 2 MyNotifi RX - small MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart phone via an app (iOS or android). All data is sent by wifi to a HIPAA controlled server for real time or accumulated time review by the provider. MyNotifiRX can be used to meet the rehabilitation needs of any extremity after injury. It can be used both pre and post-operatively to meet a patient’s rehabilitation needs. It is designed for acute or chronic use especially in patients at high risk for falls. As an added feature it is designed with a fall detection algorithm to alert designated care givers in the case of an emergency independent of a patient’s ability to respond.It is designed with two functions.1) In patients who are evaluated to be at risk for falls, MyNotifi can act as a Fall protection device and monitor. It has a built in algorithm to detect when a possible fall occurs and alerts those that the wearer has designated that an issue has occurred. It is also imbedded with the OTAGO exercise protocol https://www.apta.org/PTinMotion/NewsNow/?blogid=10737418615&id=10737430053 ) which is clinically proven to help prevent falls by improving balance. Long term remote monitoring of patients to assist, adjust, advance or correct exercise regimen is possible. Even more important, it can serve as a means to catch early deterioration of function and signal the need for intervention before an accident occurs.2) With its magnetic strip and extension band, it can be placed on any extremity to record an exercise regimen programmed by the provider. There is a library of over 40 APTA exercises (attach sheet) that can be selected.It is recommended for use in upper extremity patients for both nonoperative and post-operative rehabilitation. MyNotifi is best suited in the lower extremity for the rehab of non surgical patients. The addition of a monitor to measure heart rate and blood oxygenation during exercise adds to patient safety and serves as a measure of physical exertion during KQX Goniometer, Ac-Powered 1 MyNotifi Rx
16 00850023296016 Version 2 MyNotifi RX - medium MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart phone via an app (iOS or android). All data is sent by wifi to a HIPAA controlled server for real time or accumulated time review by the provider. MyNotifiRX can be used to meet the rehabilitation needs of any extremity after injury. It can be used both pre and post-operatively to meet a patient’s rehabilitation needs. It is designed for acute or chronic use especially in patients at high risk for falls. As an added feature it is designed with a fall detection algorithm to alert designated care givers in the case of an emergency independent of a patient’s ability to respond.It is designed with two functions.1) In patients who are evaluated to be at risk for falls, MyNotifi can act as a Fall protection device and monitor. It has a built in algorithm to detect when a possible fall occurs and alerts those that the wearer has designated that an issue has occurred. It is also imbedded with the OTAGO exercise protocol https://www.apta.org/PTinMotion/NewsNow/?blogid=10737418615&id=10737430053 ) which is clinically proven to help prevent falls by improving balance. Long term remote monitoring of patients to assist, adjust, advance or correct exercise regimen is possible. Even more important, it can serve as a means to catch early deterioration of function and signal the need for intervention before an accident occurs.2) With its magnetic strip and extension band, it can be placed on any extremity to record an exercise regimen programmed by the provider. There is a library of over 40 APTA exercises (attach sheet) that can be selected.It is recommended for use in upper extremity patients for both nonoperative and post-operative rehabilitation. MyNotifi is best suited in the lower extremity for the rehab of non surgical patients. The addition of a monitor to measure heart rate and blood oxygenation during exercise adds to patient safety and serves as a measure of physical exertion during KQX Goniometer, Ac-Powered 1 MyNotifi Rx
17 00850023296009 Version 2 MyNotifi RX - large MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart MyNotifiRX: Is a Bluetooth wearable device that interacts with a patient’s smart phone via an app (iOS or android). All data is sent by wifi to a HIPAA controlled server for real time or accumulated time review by the provider. MyNotifiRX can be used to meet the rehabilitation needs of any extremity after injury. It can be used both pre and post-operatively to meet a patient’s rehabilitation needs. It is designed for acute or chronic use especially in patients at high risk for falls. As an added feature it is designed with a fall detection algorithm to alert designated care givers in the case of an emergency independent of a patient’s ability to respond.It is designed with two functions.1) In patients who are evaluated to be at risk for falls, MyNotifi can act as a Fall protection device and monitor. It has a built in algorithm to detect when a possible fall occurs and alerts those that the wearer has designated that an issue has occurred. It is also imbedded with the OTAGO exercise protocol https://www.apta.org/PTinMotion/NewsNow/?blogid=10737418615&id=10737430053 ) which is clinically proven to help prevent falls by improving balance. Long term remote monitoring of patients to assist, adjust, advance or correct exercise regimen is possible. Even more important, it can serve as a means to catch early deterioration of function and signal the need for intervention before an accident occurs.2) With its magnetic strip and extension band, it can be placed on any extremity to record an exercise regimen programmed by the provider. There is a library of over 40 APTA exercises (attach sheet) that can be selected.It is recommended for use in upper extremity patients for both nonoperative and post-operative rehabilitation. MyNotifi is best suited in the lower extremity for the rehab of non surgical patients. The addition of a monitor to measure heart rate and blood oxygenation during exercise adds to patient safety and serves as a measure of physical exertion du KQX Goniometer, Ac-Powered 1 MyNotifi Rx
Other products with the same Product Code "IKK"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10850390007816 LE1 A recumbent, closed-chain exercise device that provides eccentric (negative) res A recumbent, closed-chain exercise device that provides eccentric (negative) resistance to lower extremity motion. It also measures strength and dynamic workload through its computer interface. Eccentron BTE TECHNOLOGIES, INC.
2 10850390007427 MCU 2 A rehabilitation device for neck strengthening exercises, as well as measurement A rehabilitation device for neck strengthening exercises, as well as measurement of cervical spine range of motion and strength. Neck musculoskeletal measurements can be taken for flexion, extension, lateral flexion, rotation, and for combined planes. MCU Multi-Cervical Unit BTE TECHNOLOGIES, INC.
3 10850390007380 Prism1 A rehabilitation system used to quantify muscle strength and range of motion, as A rehabilitation system used to quantify muscle strength and range of motion, as well as quantify compound physical abilities needed for the performance of functional tasks. Prism BTE TECHNOLOGIES, INC.
4 10850390007373 Evaluator EV A portable measurement system for quantifying musculoskeletal strength and range A portable measurement system for quantifying musculoskeletal strength and range of motion. Various EV versions are available that are different configurations of the same medical device model. Evaluator BTE TECHNOLOGIES, INC.
5 10850390007366 Evaluator EVJ A portable measurement system for quantifying musculoskeletal strength and range A portable measurement system for quantifying musculoskeletal strength and range of motion. EVJ BTE TECHNOLOGIES, INC.
6 10850390007359 1 A rehabilitation system used to quantify muscle strength and range of motion, as A rehabilitation system used to quantify muscle strength and range of motion, as well as quantify compound physical abilities needed for the performance of functional tasks. Provider Test Kit (PTK) BTE TECHNOLOGIES, INC.
7 10850390007342 EV2 Evaluator EV2 BTE TECHNOLOGIES, INC.
8 10850390007335 Evaluator A portable measurement system for quantifying musculoskeletal strength and range A portable measurement system for quantifying musculoskeletal strength and range of motion. Evaluator BTE TECHNOLOGIES, INC.
9 10850390007328 EvalTech A rehabilitation system used to quantify muscle strength and range of motion, as A rehabilitation system used to quantify muscle strength and range of motion, as well as quantify compound physical abilities needed for the performance of functional tasks. EvalTech BTE TECHNOLOGIES, INC.
10 10850390007311 ER ER BTE TECHNOLOGIES, INC.
11 09120077180076 R1 The LEXO is a mechatronic therapy system for body weight-supported gait rehabili The LEXO is a mechatronic therapy system for body weight-supported gait rehabilitation of patients with a limited ability to walk. LEXO TYROMOTION GMBH
12 08800043810121 MW-V100 Morning Walk CUREXO, INC.
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14 08054701850022 huno s APC0000404 huno s is a robotic medical device for functional sensorimotor rehabilitation an huno s is a robotic medical device for functional sensorimotor rehabilitation and evaluation of the lower limbs and trunk huno s MOVENDO TECHNOLOGY SRL
15 08054701850015 huno APC0000403 huno is a robotic medical device for functional sensorimotor rehabilitation and huno is a robotic medical device for functional sensorimotor rehabilitation and evaluation of the lower limbs and trunk huno MOVENDO TECHNOLOGY SRL
16 08054701850008 hunova APC0000400 hunova is a robotic medical device for functional sensorimotor rehabilitation an hunova is a robotic medical device for functional sensorimotor rehabilitation and evaluation of the lower limbs and trunk hunova MOVENDO TECHNOLOGY SRL
17 08054329990001 ICONE Robotic system for neurorehabilitation and rehabilitation of the upper limbs and Robotic system for neurorehabilitation and rehabilitation of the upper limbs and shoulders of patients with neuromotor disabilities. Heaxel HEALTH PIXEL SRL
18 07640174660254 Pro 32001 Lokomat HOCOMA AG
19 07640174660247 Pro 32000 Lokomat HOCOMA AG
20 07640174660223 Nanos V1.2 31002 Lokomat HOCOMA AG
21 07640174660216 Nanos V1.2 31001 Lokomat HOCOMA AG
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41 07640174420032 G-EO Robotic-assisted gait trainer G-EO REHA TECHNOLOGY AG
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43 07640174420018 G-EO System Robotic-assisted gait trainer G-EO System REHA TECHNOLOGY AG
44 07290017844114 09 REOGO005SYS The ReoGoTM therapy platform is a computerized robotics-based system for retrain The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients with motor limitations, recovering from CVA or other neuromuscular conditions. The Motorika ReoGo™ System is rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints specifically designed to prevent the adhesion and contracture of joints, to improve the patients’ range of motion and functional capabilities of the upper extremity. REOGO MOTORIKA MEDICAL (ISRAEL) LTD
45 07290017844107 08 REOGO005SYS The ReoGoTM therapy platform is a computerized robotics-based system for retrain The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients with motor limitations, recovering from CVA or other neuromuscular conditions. The Motorika ReoGo™ System is rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints specifically designed to prevent the adhesion and contracture of joints, to improve the patients’ range of motion and functional capabilities of the upper extremity. REOGO MOTORIKA MEDICAL (ISRAEL) LTD
46 06972204540016 Fourier M2 Fourier M2/Fourier M2 Kids based on force feedback and other core technologies, Fourier M2/Fourier M2 Kids based on force feedback and other core technologies, provides multiple training modes, which meet all assessment and training demands of the patients with upper limb dysfunction from flaccid paralysis phase to recovery stage.Fourier M2/Fourier M2 Kids has therapeutic games that provide real-time trajectory feedback via a monitor, which motivate users to train with more immersion. The training trajectory can be customised by using the ‘teaching mode’ which gives the therapist more flexibility to create the training plan. Fourier M2/Fourier M2 Kids also can evaluate the user’s training outcomes including the movement trajectory, movement velocity, movement torque, range of motion, muscle strength and active-passive ratio. ®Fourier SHANGHAI FOURIER INTELLIGENCE CO., LTD
47 05060481692410 P100 The unique electronic pinchmeter has a low profile design that enables the resea The unique electronic pinchmeter has a low profile design that enables the researcher to accurately quantify pinch strength at closer to end range than any other device. This product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13 Biometrics Ltd Pinchmeter BIOMETRICS LIMITED
48 05060481692403 G100 The Biometrics Dynamometer utilises precision load cell technology to increase t The Biometrics Dynamometer utilises precision load cell technology to increase the sensitivity and accuracy of measurement of even very low grip strength forces. This product is independently tested and certified to EN 60601-1:1990 including Amendments A1, A2 and A13 Biometrics Ltd Dynamometer BIOMETRICS LIMITED
49 05060481692199 K800 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 K800 Amplifier BIOMETRICS LIMITED
50 05060481692052 DLK900 DataLINK DLK900 - metal connectors 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. DataLINK DLK900 BIOMETRICS LIMITED