Fda/Cdrh; Ised; Tüv Süd; Iso - Siemens RUGGEDCOM RS920L Installation Manual

6.1.4

FDA/CDRH

This device meets the requirements of the following U.S. Food and Drug
Administration (FDA) standard:
•
6.1.5

ISED

This device is declared by Siemens Canada Ltd. to meet the requirements of the
following ISED (Innovation Science and Economic Development Canada) standard:
•
6.1.6 TÜV SÜD
This device is certified by TÜV SÜD to meet the requirements of the following
standards:
•
•
6.1.7

ISO

This device was designed and manufactured using a certified ISO (International
Organization for Standardization) quality program that adheres to the following
standard:
•
6.1.8

ACMA

This device meets the requirements of the following Australian Communications and
Media Authority (ACMA) standards under certificate ABN 98 004 347 880:
•
•
•
RUGGEDCOM RS920L
Installation Manual, 11/2022, C79000-G8976-1032-11
Title 21 Code of Federal Regulations (CFR) – Chapter I – Sub-chapter J –
Radiological Health
CAN ICES-3 (A)/NMB-3 (A)
CAN/CSA-C22.2 NO. 62368-1
Information Technology Equipment – Safety – Part 1: General Requirements (Bi-
National standard, with UL 62368-1)
UL 62368-1
Information Technology Equipment – Safety – Part 1: General Requirements
ISO 9001:2015
Quality management systems – Requirements
Radiocommunications (Compliance Labelling – Devices) Notice 2014 made
under Section 182 of the Radiocommunications Act 1992
Radiocommunications Labelling (Electromagnetic Compatibility) Notice 2008
made under Section 182 of the Radiocommunications Act 1992
Radiocommunications (Compliance Labelling – Electromagnetic Radiation)
Notice 2003 made under Section 182 of the Radiocommunications Act 1992
Certification
6.1.4 FDA/CDRH
33