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The manufacturer assumes no liability for damage caused by, or any risks arising from, use
of the microscopes for purposes other than those for which they are intended, or not using
the microscopes within the specifications of Leica Microsystems CMS GmbH. In such cases,
the Declaration of Conformity shall be invalid.
2.4 Conformity
This device has been tested and meets the requirements of the following standards:
IEC/EN 61010-1
"Safety requirements for electrical equipment for measurement, control
and laboratory use"
IEC/EN 60825-1
"Safety of laser products, Part
1: Equipment classification, requirements and user's guide"
IEC/EN 61326
"Electrical Equipment for Measurement, Control and Laboratory Use
−
EMC Requirements" (Class A).
This is a Class A instrument for use in buildings that do not include
domestic premises and buildings not directly connected to a low-
voltage power supply network that supplies buildings used for
domestic purposes.
IEC/EN 61000-3-2
"Electromagnetic Compatibility (EMC)"
Part 3-2: Limits — Limits for harmonic currents
IEC/EN 61000-3-3
"Electromagnetic Compatibility (EMC)"
Part 3-3: Limits — Limitation of voltage fluctuations and flicker in low-
voltage supply systems.
The declaration of conformity for the system is located in the appendix of this operating
manual.
For use in the USA:
CDRH 21 CFR 1040.10:
U.S. laser products Food and Drug Administration (FDA)
(”Complies with FDA performance standards for laser products
except for deviations pursuant to laser notice No. 50, dated 26
July, 2001.
For the USA (area of validity of the CDRH/FDA), the designations of the laser class are to be
changed in the text from 3B to IIIb and Class 4 to IV.
