INOXPA PHARMAVALVE, Installation, Service & Maintenance Manual

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EC DECLARATION OF CONFORMITY
(In accordance with Directive 98/37/EC, annex II, part A)
We, the manufacturer:
INOXPA, S.A.
c/ Telers, 54
17820 Banyoles (Girona) - SPAIN
Hereby declare that the products
VALVE PHARMAVALVE 2009
Name Type
Year of
Manufacture
conform with the provisions of the Council Directives:
Machine Directive 98/37/EC, and comply with the essential requirements of said
Directive and the harmonised standards:
UNE-EN ISO 12100-1/2:2003
UNE-EN 953:1997
UNE-EN 563/A1/AC:2000
Pressure equipment directive 97/23/EC, the stated equipment has been designed
and manufactured in accordance with the requirements of this Directive.
Max working pressure: DN 6 /
¼
” a DN 80 / 3” = 7 bar
Diameter:
DN 25
Equipment category: SEP = Sound Engineering Practice, determined according to Article 3, Section
1.3.a, first paragraph, annex II, table 6
This material should not have the CE marking.
Diameter:
DN 25 < X < or = DN 100
Equipment category: Category I, determined according to Article 3, Section 1.3.a, first paragraph,
annex II, table 6
This material MUST have the CE marking.
Conformity Evaluation Module: Module A
In conformity with
Regulation (CE) No. 1935/2004 on materials and objects intended to come into
contact with foodstuffs (repealing 89/109/EEC), in accordance with which the materials in contact with
the product do not transfer its constituents to the foodstuffs in quantities large enough to put human
health at risk.
Declaration of Incorporation
(Directive 98/37/EC, annex II, part B)
:
The aforementioned equipment shall not be commissioned until the machine in
which they will be incorporated has been declared as being in conformity with the
Machine Directive.
Banyoles, September 2009