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6
Safety
This manual contains information and warnings, which must be followed to ensure
the safe performance of HI-PRO 2. Local government rules and regulations, if applic-
able, should also be followed at all times.
6.1
HI-PRO 2 symbols
18
Complies with Type BF requirements of IEC 60601-
1:2005+AMD1:2012 and EN 60601-1:2006+A1:2013.
Class II equipment
Follow instructions for use.
Consult user manual for warnings and cautions.
Complies with Medical Devices Directive 93/42/EEC and
RoHS Directive (2011/65/EC).
Complies with Medical Devices Directive 93/42/EEC and
RoHS Directive (2011/65/EC). (For accessories only)
Manufacturer.
Serial number
Catalog/product number
Authorized representative in the European Community. (If
applicable for accessories only)
Otometrics - HI-PRO 2
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