Instruction Manual
K SERIES Cryostorage System
IM: CryoCeK
Revision: 02
Approved by: CB
Page
63
of
87
10 MANUFACTURER'S DECLARATION
This Worthington Industries K SERIES Cryostorage System is manufactured by:
Worthington Cylinders GmbH
Beim Flaschenwerk 1
A-3291 Kienberg bei Gaming / Austria
Tel
+43 7485 606 0
Fax
+43 7485 606 100
As the manufacturer we declare under our sole responsibility that the
Worthington Industries K SERIES Cryostorage System
is a class IIa medical device
and complies with the EU Directive
93/42/EEC (Medical Device Directive).
This conformity is indicated by the CE mark followed by the registration number 0044 of the notified
body TÜV Nord Cert GmbH, Langemarckstraße 20, 45141 Essen, Germany.
This Worthington Industries K SERIES Cryostorage System complies with the following EU Directives
WEEE - Directive 2012/19/EU (Waste of Electrical and Electronic Equipment)
RoHS 2 - Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic
Equipment)
NOTE
A copy of the Declaration of Conformity is supplied with the K SERIES Cryostorage System
and is also available upon request.