Indications for use:
The use of electrostimulation equipment is indicated in the treatment of most injuries and diseases of the musculoskeletal system, as well as in postoperative treatment after joint operations and in the treatment of a number of pain indications.
As for the NMES device, the indications refer to the following conditions:
- Delay or prevention of muscle atrophy
- Maintain or increase the range of motion
- Muscle ”re-education”
- Relaxation of muscle spasms
- Promotion of local blood circulation
As for the TENS device, the indications relate to the following conditions:
- Reduction and treatment of symptomatic chronic pain
- Treatment of postoperative and post-traumatic acute pain
- Relieving pain associated with arthritis
As a device for pulsed current, the indications relate to the following conditions:
- Reduction of edema (under a negative electrode)
- Relieving muscle spasm
- Affecting local blood circulation (under a negative electrode)
- Delay or prevention of muscle atrophy
- Improving the motor control function
- Improve or maintain range of motion
Channels | 4 |
Constant Current | Up to a resistance of Max 1300 Ohm/channel |
Maximum pulse intensity | 120 mA |
Pulse width | 30 to 400 μs |
Pulse frequency | 1 to 150 Hz |
MDD | Class IIa |
IP class | IP22 |
Applied part | Type BF Comply with safety tests: IEC 60601-1, IEC 60601-1-2, IEC 60601-2-10 |
Battery | 941213: Nickel metal hydride (NiMH) 4.8 V 2000 mA/h |
Dimensions | 138x95x33mm |
Weight | 300g (battery included) |
Dimensions | 138x95x33mm |
Additional information:
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