PowerDot PD-01 Instruction Manual page 30

Limitations: equipment is not suitable for use in the environments with a high concentration of oxygen
and/or flammable liquids and/or flammable gas; do not use with equipment for electro surgery or short‐
wave or microwave therapy.
STANDARDS
PowerDot is based directly on medical technology.
To guarantee your safety, the design, manufacturing and distribution of PowerDot are in conformity
with the requirements of the European Medical Device Directive 94/42/EEC.
The device is in conformity with the number of internationally recognized standards: standard for
general safety rules for electromedical devices IEC 60601‐1, the standard for electromagnetic
compatibility IEC 60601‐1‐2, the standard for medical electrical equipment used in the home healthcare
environment IEC 60601‐1‐11 and the standard for safety rules for nerve and muscle stimulators IEC
60601‐2‐10.
Directive 2002/96/CEE Waste electrical and electronic equipment (WEEE).
IP Rating IP22
FCC and EN300328 compatibility
The device complies with Part15 of FCC rules. Operation is subject to the following conditions:
a. This device may not cause harmful interference, and
b. This device must accept any interference received, including interference that may cause undesired
operation.
FCC ID:
2AC2KPD001201400SMT
Bluetooth Smart Ready compatibility
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