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800581-2.11 NeurOne System User Manual.doc
1.2 Symbols Used with the Device
The device is CE-marked for the conformity to Council Directive 93/42/EEC as amended by the
Directive 2007/47/EC regarding medical devices.
The device is equipped with type BF applied parts fulfilling the EN 60601-1 (IEC60601-1)
standard.
The enclosure protection class is IP20 according to EN60529.
Caution.
Warning.
Follow operating instructions.
~
Alternating current (A.C.)
Direct current (D.C.)
ESD sensitive connector.
For EU only: This symbol indicates that this device shall be disposed according to European
Union directive 2002/96/EC on Waste Electrical and Electronic Equipment (WEEE).
1.3 User Responsibility
This product shall be assembled, operated, maintained and repaired in accordance
with the instructions provided.
A defective product should not be used. Parts that are broken, worn, missing,
incomplete, distorted or contaminated should be replaced immediately. Should any
repair or replacement become necessary, we recommend that the device is delivered
to your local distributor or Bittium Biosignals Ltd for service.
The user of the product is solely responsible for any malfunction resulting from
improper use, faulty maintenance, improper repair, damage or alteration by anyone
other than Bittium Biosignals Ltd or their authorized service personnel.
NeurOne system does not provide any automatic analysis or
diagnosis.
