GE AKTA ready XL User Manual

9.5.2 European Union and European Economic Area
I
ntroduction
This section describes regulatory information for the European Union and European
Economic Area that applies to ÄKTA ready XL.
Conformity with EU Directives
See the EU Declaration of Conformity for the directives and regulations that apply for
the CE marking.
If not included with the product, a copy of the EU Declaration of Conformity is availa-
ble on request.
CE marking
The CE marking and the corresponding EU Declaration of Conformity is valid for the
i
nstrument when it is:
• used according to the Operating Instructions or user manuals, and
• used in the same state as it was delivered, except for alterations described in the
Operating Instructions or user manuals.
9 Reference information
9
.5 Regulatory information
9.5.2 European Union and European Economic Area
ÄKTA ready XL Operating Instructions 29281616 AE 159
*** TeDIS Valid on Date Printed Printed on: 15-09-2023 11:27:35 ***

GE AKTA ready XL Specifications

General

Brand	GE
Model	AKTA ready XL
Category	Medical Equipment
Language	English