Technical Specifications - Revitive ProHealth RLV Bedienungsanleitung

EN

Technical Specifications

Name of product
Model
Frequency
Output current
Weight
Dimensions
Power consumption
AC adaptor
Power source
Input (adaptor used)
Output
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
This describes situations where you should not use REVITIVE
Warnings and Cautions
Make sure you understand these before using the REVITIVE
Power
Time Remaining
24
4426_IFU01_15927663.indd 24-25
REVITIVE ProHealth
RLV
1Hz – 50Hz
Max 8.5mA
1.13kg
Ø 355 mm x 77(D) mm
5W
CE Approved
100-240V AC ( ), 50/60Hz, 0.18A
5V ( ) DC ,1.0A
S/N
#YYYYMMXXXXX
REF
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 Authorised Representative
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
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.
EN
90% 70°C
20%
-20°C
1060 hPa
500 hPa
75%
40°C
30% 10°C
1060 hPa
700 hPa
25
22/02/2019 12:05