GE FineLINE 35 oligo, Operating Instructions Manual

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1 Introduction
1.2 Regulatory information
8
FineLINE 35 oligo column Operating Instructions 28-9649-57 AA
CE marking
The CE marking and the corresponding Declaration of Conformity is valid for the
instrument when it is:
• used as a stand-alone unit, or
• connected to other CE-marked instruments, or
• connected to other products recommended or described in the user
documentation, and
• used in the same state as it was delivered from GE Healthcare, except for
alterations described in the user documentation or explicitly authorized by GE
Healthcare.
Regulatory compliance of
connected equipment
Any equipment connected to FineLINE 35 oligo column should meet the safety
requirements of relevant harmonized standards. Within the European Union, connected
equipment must be CE-marked.