Certification
6.1.4 FDA/CDRH
IMPORTANT
Changes or modifications not expressly approved by the party responsible for com-
pliance could void the user's authority to operate this device.
6.1.4
FDA/CDRH
This device meets the requirements of the following U.S. Food and Drug Administra-
tion (FDA) standard:
• Title 21 Code of Federal Regulations (CFR) – Chapter I – Sub-chapter J – Radiolog-
ical Health
6.1.5
ISED
This device is declared by Siemens AG to meet the requirements of the following
ISED (Innovation Science and Economic Development Canada) standard:
• CAN ICES-3 (A)/NMB-3 (A)
6.1.6
TÜV SÜD
This device is certified by TÜV SÜD to meet the requirements of the following stan-
dards:
•
CAN/CSA-C22.2 NO. 60950-1
Information Technology Equipment – Safety – Part 1: General Requirements (Bi-
National standard, with UL 60950-1)
•
UL 60950-1
Information Technology Equipment – Safety – Part 1: General Requirements
6.1.7
ACMA
This device meets the requirements of the following Australian Communications and
Media Authority (ACMA) standards under certificate ABN 98 004 347 880:
• Radiocommunications (Compliance Labelling – Devices) Notice 2014 made un-
der 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) No-
tice 2003 made under Section 182 of the Radiocommunications Act 1992
• Telecommunications Labelling (Customer Equipment and Customer Cabling) No-
tice 2001 made under Section 407 of the Telecommunication Act 1997
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