TensCare Sports TENS 2 Mode D'emploi page 6

Catalogue Number: indicates the manufacturer's catalogue number so that the device
can be identified.
Atmospheric Pressure: indicates the atmospheric limits to which the medical device can
be safely exposed.
Manufacturer Symbol
Date of Manufacture: indicates the date which the medical device was manufactured.
This is included within the serial number found on the device (usually on the back of the
device), either as "E/Year/Number" (YY/123456) or "E/Month/Year/Number"
(MM/YY/123456).
CE Mark
Medical Device
This medical device is indicated for home use.
This medical device is not water resistant and should be protected from liquids.
The first number 2: Protected against access to hazardous parts with a finger, and the
jointed test finger of 12 mm ø, 80 mm length, shall have adequate clearance from
hazardous parts, and protected against solid foreign objects of 12.5 mm ø and greater.
The second number 2: Protected against vertically falling water drops when enclosure is
tilted up to 15˚. Vertically falling drops shall have no harmful effects when the enclosure is
tilted at any angle up to 15˚ on either side of the vertical.
Notes are used to provide clarification or recommendation.
A Warning is used when failure to follow the instructions may result in serious injury or.
death
A Caution is used when failure to follow the instructions may result in a minor or
moderate injury, or damage to the device or other property.
A Contraindication is used when a device should not be used because the risk of use
clearly outweighs any foreseeable benefits and may result in serious injury or death.
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