Table of Contents
Advertisement
Certification
6.1.3 European Commission (EC)
6.1.3
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:
•
•
•
•
•
The device is marked with a CE symbol and can be used throughout the European
community.
6.1.4
FDA/CDRH
This device meets the requirements of the following U.S. Food and Drug
Administration (FDA) standard:
•
6.1.5
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.
48
EN 62368-1
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 63000
Technical Documentation for the Assessment of Electrical and Electronic
Products with Respect to the Restriction of Hazardous Substances
CISPR 32/EN 55032
Electromagnetic Compatibility of Multimedia Equipment – Emission
Requirements
Title 21 Code of Federal Regulations (CFR) – Chapter I – Sub-chapter J –
Radiological Health
RUGGEDCOM RX5000
Equipment Manual, 11/2023, C79000-G8976-1058-15
Advertisement
Table of Contents
