Chapter 6
Certification
RUGGEDCOM MX5000
Installation Guide
36
European Commission (EC)
Section 6.1.2
European Commission (EC)
This device is declared by Siemens Canada Ltd to comply with essential requirements and other relevant provisions
of the following EC directives:
•
EN 60950-1
Information Technology Equipment – Safety – Part 1: General Requirements
•
EN 61000-6-2
Electromagnetic Compatibility (EMC) – Part 6-2: Generic Standards – Immunity for Industrial Environments
•
EN 60825-1
Safety of Laser Products – Equipment Classification and Requirements
•
EN 55022
Information Technology Equipment – Radio disturbance characteristics – Limits and methods of measurement
•
EN 50581
Technical Documentation for the Assessment of Electrical and Electronic Products with Respect to the Restriction
of Hazardous Substances
The device is marked with a CE marking and can be used throughout the European community.
A copy of the CE Declaration of Conformity is available from Siemens Canada Ltd. For contact information, refer to
Section 6.1.3
FCC
This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to Part
15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference when
the equipment is operated in a commercial environment.
This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in
accordance with the instruction manual, may cause harmful interference to radio communications. Operation of
this equipment in a residential area is likely to cause harmful interference in which case the user will be required
to correct the interference on his own expense.
Section 6.1.4
FDA/CDRH
This device meets the requirements of the following U.S. Food and Drug Administration (FDA) standard:
• Title 21 Code of Federal Regulations (CFR) – Chapter I – Sub-chapter J – Radiological Health
