CE marking
The CE marking and the corresponding EU Declaration of Conformity is valid for the in-
strument when it is:
•
used according to the Operating Instructions or user manuals, and
•
used in the same state as it was delivered from GE, except for alterations described
in the Operating Instructions or user manuals.
1.3.2
Eurasian Customs Union
Introduction
This section contains additional regulatory information to comply with the Eurasian
Customs Union technical regulations.
Manufacturer and importer
information
The table below summarizes the manufacturer and importer information required by
the Eurasian Customs Union.
Information
Requirement
See Manufacturing information
Name and address of manufacturer
Telephone: + 46 771 400 600
Telephone number of manufacturer
GE Healthcare LLC
Importer and/or company for obtain-
ing information about importer
GE Healthcare Life Sciences
Presnenskaya nab., 10C, 12th floor
RU-123 317 Moscow, Russian Federation
Telephone 1: + 7 495 411 9714
Fax nr: + 7 495 739 6932
Email: [email protected]
8
Monitor UV-900 Operating Instructions 28962214 AD
1 Introduction
1.3 Regulatory information
1.3.1 EU Directives