Finometer® Model-2 User’s Guide 79
9 Specifications
T s /EEC (Medical
Device Directive) and the Euro
1-1, EN 60601-1-2.
Man s B.V.
9 0677
Im pecifications may be subject to change without notice.
hi device fulfills the provisions of the EC directive 93/42
pean Standards EN 60601-1; EN 60601-
ufacturer: Finapres Medical System
Paasheuvelweg 34a
1105 BJ Amsterdam ZO
The Netherlands
Phone: + 31 20 609 0974
Fax: + 31 26 60
E-mail: info@finapres.com
portant note: S
034
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