Quick Guide
2
Errors and Suggestions
If you spot any mistakes in this online help or if you have any suggestions for improvement,
please contact MetaSystems in Germany.
Compliance Notice
Systems by MetaSystems have been designed, produced and tested to meet the require-
ments regarding:
Directive 2006/95/EC for electrical equipment
designed for use within certain voltage limits.
EN 61010-2-101:2002 Safety requirements for
electrical equipment for measurement, con-
trol, and laboratory use – Part 2-101: Particular
requirements for in vitro diagnostic (IVD) med-
ical equipment (IEC 61010-2-101:2002 (Modi-
fied)).
a Electromagnetic Compatibility
(EMC)
Directive 2014/30/EU for electromagnetic com-
patibility.
EN 61326-2-6:2006 Electrical equipment for
measurement, control and laboratory use –
Part 2-6: Particular requirements – In vitro di-
agnostic (IVD) medical equipment (IEC 61326-2-
6:2005).
And meet the requirements of the
EU directive 98/79/EC for IVD products (In Vitro
Diagnostics)
Instrumentation identification marking
This product complies with the requirements in the EU directive 98/79
EC on in vitro diagnostic medical devices.
For in vitro diagnostic use.
Consult instructions for use.
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