ГОСТ Р 57386—2017
Библиография
[1J ISO 31 (all parts) Quantities and units
(2} ISO 13485 Medical devices — Quality management systems — Requirements tor regulatory purposes
(3] ISO 14630 Non-active surgical implants — General requirements
(4] ISO 14708-1 Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety,
marking and for information to be provided by the manufacturer Guidance on the analysis of risks associated with the use
of implants can be found in the following document
(5] ISO 14971 Medical devices — Application of risk management to medical devices
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