Gilson PIPETMAN F Series, Manual

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1
ENGLISH
Ec dEcLaratIon of conformIty
Pipetman® F
F2, F5, F10, F20, F25, F50, F100,
F200, F250, F300, F400, F500, F1000, F5000
98/79/EC*
on In Vitro Diagnostic
Medical Devices
comply with the requirements
of the following European
Directives:
Villiers-le-Bel, September 14
th
, 2005
A. El Sayed H. Ledorze
General Manager Quality Manager
GILSON S.A.S.
19, avenue des Entrepreneurs
BP. 145 - 95400 Villiers-le-Bel (France)
Tel.: +33(0)1 34 29 50 00
Fax: +33(0) 1 34 29 50 20
www.gilson.com
* Annex III, self-declared
The company,
Hereby certifies on its sole responsibility that the products
listed below: