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Functional safety of electrical, electronic, programmable electronic safety-related systems. Part 1. General requirements
Document status: Replaced by GOST R IEC 61508-1-2012
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 1. Terms, definitions and general requirements
Document status: Replaced by GOST R ISO 18113-1-2024
Wheelchairs. Type classification based on appearance characteristics
Document status: Cancelled
X-ray image intensifiers for medical apparatus. General technical requirements. Methods of test
Document status: Active
Vascular stents. Technical requirements
Document status: Replaced by GOST R ISO 25539-2-2012