Image 1 of 5
Image 2 of 5
Image 3 of 5
Image 4 of 5
Image 5 of 5
FDA Cleared
SCENAR™ devices are FDA-cleared for the treatment and management of acute and chronic pain, including post-surgical and post-traumatic pain.
CE Marked & ISO Certified
SCENAR holds CE certification for pain relief in the EU and meets ISO 9001 and ISO 13485 international quality management standards for medical devices.
Device Specifications
- Power Supply: 4 x AAA batteries
- Frequency Range: 15 Hz – 350 Hz
- Amplitude & Frequency Modulation: Multiple preset and customizable modes
- Display: LCD (varies by model)
- Weight: ~0.4 kg; Dimensions: 190 x 70 x 40 mm
Safety
SCENAR is non-invasive, with no known side effects. It is contraindicated only for patients with cardiac pacemakers or certain neurological conditions.
Warranty
Devices include a two-year limited warranty from the manufacturer.
Global Compliance
SCENAR is registered and approved for medical use in over 36 countries, including the US, EU, Israel, Australia, and more.