Siemens RUGGEDCOM RS950G, Руководство по установке

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Chapter 6
Certification
RUGGEDCOM RS950G
Installation Guide
28 European Union (EU)
Section 6.1.2
European Union (EU)
This device is declared by Siemens Canada Ltd to comply with essential requirements and other relevant provisions
of the following EU 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 50581
Technical Documentation for the Assessment of Electrical and Electronic Products with Respect to the Restriction
of Hazardous Substances
• EN 55032
Information Technology Equipment – Radio Disturbance Characteristics – Limits and Methods of Measurement
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
“Contacting Siemens” .
Section 6.1.3
FCC
This device 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 device 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 users will be required to
correct the interference at their own expense.
IMPORTANT!
Changes or modifications not expressly approved by the party responsible for compliance could void
the user's authority to operate this device.
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