Actegy REVITIVE CIRCULATION BOOSTER Manuel De L'utilisateur page 14

EN
Technical Specifications
Symbols
Complies with European Medical Devices Directive (93/42/EEC)
Device serial 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 the Revitive
Power
Time Remaining
Intensity Level
Center Positive Polarity
Class II medical electrical equipment double insulated
Type BF medical electrical equipment
Legal manufacturer of the device
EU/EC European Authorized Representative
UK Conformity Assessed
Product conforms to all applicable U.K. legislative requirements.
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.
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Consult instructions for use
LOT
#YYYYMMXXXXX
The Waste Electrical and Electronic Equipment Directive
(WEEE Directive).
At the end of the product lifecycle, do not throw this product
REF
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
YYYY MM DD
90%
70°C
20%
-20°C
1060 hPa
500 hPa
75%
70°C
30% -20°C
1060 hPa
700 hPa
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