22
PIPETMAN
®
P
ec decLaratIon oF conFormIty
PIPetman® P
P2, P10, P20, P100, P200,
P1000, P5000 and P10ml
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:
Summary of Contents for PIPETMAN P Series
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