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ManaFlexx 2 – Rx Only

Original price was: $138.00.Current price is: $84.00.

Requires Prescription

SKU: MF002-RX Categories: , Tag:
Brand:ManaMed

RECOMMENDED FOR:

The ManaFlexx 2 Unit can achieve either NMES (Neuromuscular Electrical Stimulation) or TENS (Transcutaneous Electrical Nerve Stimulation). It is the only NMES device designed for ease of use by eliminating wires or standalone electrodes. It can be placed anyway treatment is desired.

  • No cords
  • Pads can last 30 days
  • 19 intensity levels

NMES produces a clean and complete muscle contraction. It is an effective treatment to slow or prevent muscle atrophy, re-educate paralyzed muscles, relax muscle spasms, and facilitate recovery. It can also be applied to the calf post-operatively to prevent DVTs. A NMES electrical current is stronger with a greater pulse width, to produce muscle contractions. 

  • Creates a clean and complete muscle contraction
  • Re-educates muscle
  • Slows and prevents muscle atrophy
  • Facilitates recovery
  • Relaxes muscle spasms
  • Increases local blood circulations
  • Maintains or increases range of motion
  • Can prevent venous thrombosis when used post-operatively to stimulate the calf muscles

Comparatively, TENS provides temporary pain relief. By stimulating the sensory nerves, TENS blocks pain signals and triggers endorphin production. It is a great choice for those looking to reduce their pain medication use. TENS transmits at a frequency that is below muscle contraction. 

  • Blocks pain signals
  • Triggers endorphin production

Brand

ManaMed

With extensive product and innovative offerings, ManaMed provides solutions to address the patient’s continuum of care from performance and mobility to post-operative rehabilitation. For over seven years ManaMed has been creating products that help people get back on their feet after injury or surgery, enabling them to stay active longer.

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What is the valid prescription?

To purchase any of our NMES/EMS, or IFC electrotherapy devices, a valid prescription is required because they fall into the FDA's group of Class II Devices.