Leica Biosystems SP9000 - Manuel (Page 28)

28 Mode d’emploi V 2.2 – 08/2007
. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Anne De Greef-Safft
President Biosystems Division
Leica Biosystems Nussloch GmbH
Postfach 1120
D-69222 Nussloch
October 11, 2007
We herewith declare, in exclusive responsibility, that the instrument
Leica SP9000 –
Automatic Knifesharper
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
10. EC Declaration of Conformity