Roche MagNA Pure Compact Instrument - Marks of Conformity

MagNA Pure Compact Operator’s Manual - Version 1.3
6
Marks of Conformity
The MagNA Pure Compact Instrument had been investigated according to:
䉴 IEC 61010-1, 2nd Edition ("Safety requirements for electrical equipment for
measurement, control and laboratory use; Part 1: General requirements")
䉴 EN 61326:1997 + A1:1998 + A2:2001 Class B ("Electrical equipment for measurement,
control and laboratory use - EMC requirements")
䉴 UL 61010A-1
䉴 CAN/CSA C22.2 No. 1010.1-92
The instrument has been manufactured and checked in accordance with all relevant
safety standards prior to leaving the factory. The instrument has been approved for use by
recognized testing institutions. This is confirmed by the following conformity symbols:
Equipment to be connected must fulfill the standards set by IEC 950 (Information-
security in technical equipment, including electronic business machines).
Acronym Test Symbol Testing Information
CE The instrument conforms to following directives as
issued by the European Union according to the Council
Directive 89/336/EEC (Electromagnetic Compatibility)
and 73/23/EEC (Electrical equipment for use within
certain voltage limits).
CUL Certified by the Underwriters Laboratories Inc.
Classification Note on Use with Infectious Material
The Instrument is classified as: 䉴 The Instrument may not be used to
analyze
infectious materials unless
additional safety measures to ensure
safe sample handling are taken
beforehand.
䉴 Designed for stationary operation.
䉴 Intended for worldwide use.
䉴 Intended for evaluating preprocessed
biological material.
Intended Use of the Instrument
Marks of Conformity
MagNA Pure Compact Manual.book Seite 6 Dienstag, 28. Februar 2006 4:16 16