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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, 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
EU/EC European Authorised Representative
#YYYYMMXXXXX
LOT
REF
Technical Specications
FCC mark
Certification mark employed on electronic products manufactured
or sold in the United States which certifies that the electromagnetic
interference from Revitive is under limits approved by the Federal
Communications Commission
Consult instructions for use
The Waste Electrical and Electronic Equipment Directive
(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 YYYY MM DD
Humidity, temperature and air pressure limit for storage
and transport
Humidity, temperature and air pressure limit for operating
conditions
Aer 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
Medical device does not contain natural rubber latex
Do not disassemble
-20°C
20%
70°C
90%
500 hPa
1060 hPa
10°C30%
40°C
75%
700 hPa
1060 hPa
EN
EN
4397_IFU05_17892258.indd 40-41
4397_IFU05_17892258.indd 40-41
15/02/2021 09:07
15/02/2021 09:07
21


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