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Technical Specifications
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%
Output Specifications for Transcutaneous Electrical Nerve Stimulation (TENS):
Waveform
Shape
Maximum Output Voltage
Pulse Duration
Net Charge (per pulse @ 500Ω)
Maximum Average Power Density (@ 500Ω)
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 Revitive works within its Essential Performance after a certain period of time, contact the
manufacturer
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8035_IFU01_19037975_PRINT.indd 38-39
Biphasic
Square symmetrical with polarity reversal
Foot: 26 - 35Vp
Body: 18 - 32.6Vp
Foot: 450 or 970µs
Body: 450µs
[0.001]mC
Foot: 0.414 mW/cm2
Body: 1.52-3.82 mW/cm²
Foot: 1.90 - 8.30s
Body: 1.90 -33.0s
Foot: 1.00 - 1.50s
Body: 1.00 - 47.0s
Biphasic
Rectangular
@ 500Ω
50Vp
100µs
0μC
4.19 mW/cm
2
Symbols
Complies with European Medical
Devices Directive (93/42/EEC)
UK Conformity Assessed
Product conforms to all applicable U.K. legislative
requirements.
Device serial number including
year (YYYY) and month (MM) of
manufacture can be found on the
#YYYYMMXXXXX
box and back of unit
Revitive Indication Number
Item number
Contraindications, Warnings and
Cautions
Make sure you understand these before using
Revitive
Power
Time Remaining
Intensity Level
Electrode pads indicator
Battery Indicator
Bluetooth Enabled
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
EN
Ingress Protection Rating
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.
RCM Mark
The equipment complies with Radio
Communications and EMC requirements for
Australia and New Zealand
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
Use-by date
YYYY MM DD
Humidity, temperature and air
90%
pressure limit for storage
and transport
20%
70°C
-20°C
1060 hPa
500 hPa
Humidity, temperature and air
75%
pressure limit for operating
30%
conditions
After any exposure to hot or cold temperatures
40°C
outside the specified operating range of
10 - 40°C allow the product to re-adjust to the
10°C
recommended operating temperatures to ensure
1060 hPa
continued product performance.
700 hPa
Indoor Use Only
Medical device does not contain
natural rubber latex
Do not disassemble
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