Leica Biosystems SM2500 - Handbuch (Seite 75)

10. CE-Konformitätserklärung
was developed, designed and manufactured to conform with the
•
Council Directive 73/23/EEC, (Low Voltage) and
• Council Directive 89/336/EEC, Appendix I (Electromagnetic Compatibility),
including their amendments up to the date mentioned below.
The following harmonized standards were applied:
• EN 61010-1: 2001
Safety requirements for electrical equipment for measurement, control and laboratory use -
Part 1: General requirements
• EN 61326-1:1997 + EN 61326/1:1998
Electrical equipmentl for measurement, control and laboratory use - EMC requirements -
Part 1: General requirements
• EN 61000-3-2:1995 + A1:1998 + A2:1998 + A14:2000
Electromagnetic compatibility (EMC)
Part 3-2: Limits - Limits for harmonic current emissions
• EN 61000-3-3:1995
Electromagnetic compatibility (EMC)
Part 3: Limits -
Section 3: Limitation of voltage fluctuations and flicker in low-voltage supply systems for equirement
with rated current £ 16 A
• EN 418:1992
Emergency stop equipment.
Principles for design.
• EN 1037:1995
Safety of machinery.
Prevention of unexpected start-up.
In addition, the following in-house standards were applied:
• DIN EN ISO 9001: 2000.
We herewith declare, in exclusive responsibility, that the instrument
Leica SM2500 –
Sliding Microtome
with and without SP2600 – Ultramiller Attatchment
EC Declaration of Conformity
. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Anne De Greef-Safft
President Biosystems Division
Leica Biosystems Nussloch GmbH
Postfach 1120
D-69222 Nussloch
October 11, 2007