Revitive CIRCULATION BOOSTER ESSENTIAL - Page 14

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Technical Specications
EN
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.
#YYYYMMXXXXX
LOT
REF
Symbols
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
-20°C
30%
70°C
75%
700 hPa
1060 hPa
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