Fda/Cdrh; Ised; Iso; Acma - Siemens SIMATIC NET RUGGEDCOM RS900G Equipment Manual

Changes or modifications not expressly approved by the party responsible for
compliance could void the user's authority to operate this device.
6.1.5

FDA/CDRH

This device meets the requirements of the following U.S. Food and Drug
Administration (FDA) standard:
•
6.1.6

ISED

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

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 RS900G
Equipment Manual, 10/2023, C79000-G8976-1025-10
NOTICE
Title 21 Code of Federal Regulations (CFR) – Chapter I – Sub-chapter J –
Radiological Health
CAN ICES-3 (A)/NMB-3 (A)
ISO 9001:2015
Quality management systems – Requirements
Radiocommunications (Compliance Labeling – Devices) Notice 2014 made under
section 182 of the Radiocommunications Act 1992
Radiocommunications Labeling (Electromagnetic Compatibility) Notice 2017
made under section 182 of the Radiocommunications Act 1992
Radiocommunications (Compliance Labeling – Electromagnetic Radiation) Notice
2014 made under section 182 of the Radiocommunications Act 1992
Telecommunications (Labeling Notice for Customer Equipment and Customer
Cabling) Instrument 2015 made under section 407 of the Telecommunication
Act 1997
Certification
6.1.5 FDA/CDRH
29