Fda And Iec Marks - Siemens SCALANCE XR524-8C Operating Instructions Manual

cULus Approval Hazardous Location
cULus Listed I. T. E. FOR HAZ. LOC.
Underwriters Laboratories Inc. complying with
● UL 60950-1 (Information Technology Equipment)
● ANSI/ISA 12.12.01-2007
● CSA C22.2 No. 213-M1987
Approved for use in
Cl. 1, Div. 2, GP A, B, C, D T4
Cl. 1, Zone 2, GP IIC T4
Report no. E240480
Note
Only variants with 24 VDC power supply meet the requirements of this approval.
EU declaration of conformity
You will find EC declaration of conformity for these products on the Internet pages of
Siemens Industry Online Support
(http://support.automation.siemens.com/WW/view/en/33118389/134200).
10.1

FDA and IEC marks

The following devices meet the FDA and IEC requirements listed below:
Device
SCALANCE XR524-8C
SCALANCE XR528-6M
SCALANCE XR552-12M
Note: With modular devices , the marking is on the MM900 media modules and the SFP and SFP+ transceivers.
Figure 10-1
SCALANCE XR-500
Operating Instructions, 05/2014, A5E03275845-05
Fulfills FDA and IEC requirements
FDA and IEC approvals
Certification
10.1 FDA and IEC marks
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