Technical Information

  • Microcurrent Therapy Patch Model #7500 v6.
  • See safety information.
  • Rated Output 0.5 Hz, pulsed DC waveform, 21mV@42µA under 500 ohm.
  • Store Microlief® at room temperature in a dry place.
  • Continuous operation.
  • Internally powered equipment.

 

Type BF Applied Part

 

 

Environmental Conditions that can Affect Use

Microlief® should only be used within the temperature rage of 10°- 45°C (50°-113°F) and at a relative humidity range of 20%-90%.  If the product has been stored or transported in conditions outside these ranges, keep it within recommended ranges for 30 minutes before using.

Disposal Information

This product does not contain any environmentally hazardous substances and can be disposed of normally.  The battery used in the Controller should not be mistreated.  Do not attempt to recharge, disassemble or dispose of in a fire.

Safety Testing

The Microlief MCT Patch was tested and in compliance with:

IEC 60601-1 (Ed.3) and EN 6061-1: 2006 + CORR: 2010

Medical Electrical Equipment Part 1: General Requirements for Basic Safety and Essential Performance.

EN60601-1, 3rd Edition (2012) Medical Equipment, Part 1: General
Requirements for Basic Safety and Essential Performance.

EN60601-2-10 Medical Equipment, Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators.

CAN/CSA-C22.2 No. 6060-1 (2008) Medical Electrical Equipment, Part 1: General Requirements for Basic Safety and Essential Performance.

CAN/CSA-C22.2 No. 601.2.10 (1992) Medical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators.

EN60601-1-2 (2007) Electromagnetic Emissions and Immunity Requirements for Medical Electrical Equipment.