Revitive Essential CIRCULATION BOOSTER Bedienungsanleitung Seite 11

Technical specifications
Name of product
Model
Frequency (+/-10%)
Output current
Weight (+/-0.5kg)
Dimensions
Power consumption
AC adaptor
Power source
Input (adaptor used)
Output
Service Life of Device
Period of time specified by the manufacturer during which the device
is expected to remain safe for use.
Applied parts
Part of Revitive that in normal use come into physical contact with
user to perform therapy
Output Specifications for Electrical Muscle Stimulation (EMS):
Waveform
Shape
Maximum Output Voltage (+/-15%) @500Ω
Pulse Duration (+-10%)
Net Charge @ 500Ω
Maximum Power Density @ 500Ω
ON Time (+-10%)
OFF Time (+-10%)
The values of PULSE DURATIONS, PULSE repetition frequencies and amplitudes, including any d.c. component, shall not
deviate by more than ± 20 % when measured with a load resistance within the range specified.
If confirmation is required that the Revitive works within its Essential Performance after a certain period of time, contact
the manufacturer
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Revitive Essential
RLV
Foot: 20 to 44Hz
Body: 37 to 51Hz
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
4 Years
Foot-pads - 135.5cm
2
Electrode Body Pads - 5cm x 5cm = 25cm
Biphasic
Square symmetrical with polarity reversal
Foot: 21.5Vp Body: 21.5Vp
Foot: 450 or 970µs (Mode 7) Body: 450µs
[0.001]mC
Foot: 0.19 mW/cm² Body: 1.50 mW/cm²
Foot: 1.9 - 8.3s Body: 1.9 - 6.5s
Foot: 1.00 - 1.50s Body: 1.00s
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
Revitive
Power
Time Remaining
Intensity Level
Center Positive Polarity
2
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.
Consult instructions for use
The Waste Electrical and Electronic
Equipment Directive (WEEE
Directive).
At the end of the product lifecycle, do not throw
#YYYYMMXXXXX
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.
Indoor Use Only
Medical device does not contain
natural rubber latex
Do not disassemble
EN
YYYY MM DD
90%
20%
70°C
-20°C
1060 hPa
500 hPa
75%
30%
40°C
10°C
1060 hPa
700 hPa
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