Certification
6.1.5FDA/CDRH
Note
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:
• Title 21 Code of Federal Regulations (CFR) – Chapter I – Sub-chapter J –
Radiological Health
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:
• CAN ICES-3 (A)/NMB-3 (A)
6.1.7 TÜV SÜD
This device is certified by TÜV SÜD to meet the requirements of the following
standards:
• 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
6.1.8 RRA
This device has been registered by the Korean Radio Research Agency (RRA) under
Clause 3, Article 58-2 of the Radio Waves Act. As such, the device is marked with a KC
symbol and can be used in the Republic of Korea (South Korea) as a Class A product
in a commercial, industrial or business environment.
A copy of the KC Declaration of Conformity is available from Siemens Canada Ltd..
For contact information, refer to "Contacting Siemens" (Page vii).
RUGGEDCOM RST916C
Installation Manual, 04/2023, C79000-G8976-1490-07
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