Revitive 2836AB Manuel De L'utilisateur page 21

EN
Technical Specifications
Complies with European Medical Devices Directive (93/42/EEC)
LOT and serial number of the device, including year (YYYY) and month
(MM) of production, as stated on the packaging and on the back of the
device.
Item number
Contraindications
This describes situations where you should not use REVITIVE
Warnings and Cautions
Make sure you understand these before using the REVITIVE
Power
Time Remaining
Intensity Level
EMS Mode
TENS Mode
Battery Indicator
IsoRocker® Disabler
Center Positive Polarity
Class II medical electrical equipment double insulated
Type BF medical electrical equipment
Legal manufacturer of the device
40
4397_IFU02_16220241.indd 40-41
EU/EC European Authorised Representative
LOT
#YYYYMMXXXXX
Consult instructions for use
The Waste Electrical and Electronic Equipment Directive
REF
(WEEE Directive).
At the end of the product lifecycle, do not throw this product
into normal household garbage, but take it to a collection point for the
recycling of electronic equipment
Ingress Protection Rating
Use-by date
Humidity, temperature and air pressure limit for storage
and transport
Humidity, temperature and air pressure limit for operating
conditions
After any exposure to hot or cold temperatures outside the specified
operating range of 10 - 40°C allow the product to re-adjust to the
recommended operating temperatures to ensure continued product
performance.
Indoor Use Only
Do not disassemble
Medical device does not contain natural rubber latex
EN
90%
70°C
20%
-20°C
1060 hPa
500 hPa
75%
40°C
30% 10°C
1060 hPa
700 hPa
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