34
35
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. Actegy Ltd complies with all
applicable FCC rules.
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
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
Medical device does not contain natural rubber latex
Do not disassemble
-20°C
20%
70°C
90%
500 hPa
1060 hPa
10°C
30%
40°C
75%
700 hPa
1060 hPa
Complies with European Medical Devices Directive (93/42/EEC)
UK Conformity Assessed
Product conforms to all applicable U.K. legislative requirements.
Device Lot number including year (YYYY) and month (MM) of
manufacture can be found on the box and back of unit
Item number
Contraindications, Warnings and Cautions
Make sure you understand these before using Revitive
Power
Time Remaining
Intensity Level
EMS Mode
TENS Mode
Battery Indicator
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
Symbols
Technical Specifications
5603_IFU02_17807098.indd 34-35
5603_IFU02_17807098.indd 34-35
12/01/2021 08:53
12/01/2021 08:53
