Leica Biosystems CM1100 - Příručka (Stránka 35)

35 Leica CM1100 – Kryostat
We herewith declare, in exclusive responsibility, that the instrument
Leica CM1100 – Cryostat
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 + A1: 1998 + A2: 2001 + A3: 2003
Electrical equipmentl for measurement, control and laboratory use -
EMC requirements -
Part 1: General requirements
• EN 61000-3-2: 2000
Electromagnetic compatibility (EMC)
Part 3-2: Limits - Limits for harmonic current emissions
• EN 61000-3-3: 1995 + A1: 2001
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
In addition, the following in-house standards were applied:
• DIN EN ISO 9001: 2000
Leica Microsystems Nussloch GmbH
Postfach 1120
D-69222 Nussloch
January 12, 2004
EC Declaration of Conformity
. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Dag Graupner
Managing Director
15. EC Declaration of Conformity