Owner’s Guide
35
Regulatory Information
Safety:
Complies with IEC 60601-1:2012 (tested by TUV
Singapore)
EMC:
Complies with IEC 60601-1-2:2014 (tested by EMC
Technologies, Sydney, Australia)
Equipment:
Use only with an ADInstruments 35 series PowerLab.
The PowerLab must be connected to safety earth via the
power supply cable to ensure electrical safety.
Operation:
Continuous
Body protection rating
(Applied parts only):
(BF)
Unsuitable uses:
Do not use in the presence of flammable anaesthetic - air
mixtures. Avoid operating near high voltage, RF or strong
magnetic fields that may cause interference.
Method of Disposal:
Forward to recycling centre or return to manufacturer.
This equipment is not intended to be modified or serviced by the user. No user serviceable
parts inside. Refer servicing to authorised ADInstruments service centre.
ADInstruments
reserves the right to alter these specifications at any time.
Electromagnetic Compatibility
The Bio Amps (the devices) have been tested to comply with the requirements of IEC
60601-1-2. (The relevant basic EMC standards are IEC 61000-4-2, IEC 61000-4-3, IEC
61000-4-6, IEC 61000-4-8, IEC 61000-4-11 and CISPR 11).
Emissions
•
The devices use RF energy for its internal function only. RF emissions are very
low and are not likely to cause any interference in nearby electronic equipment.
•
The devices are suitable for use in all establishments, including domestic
establishments and those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.
NOTE:
PowerLabs
provide power
to the Bio Amp
and no other
power source is
required.
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