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DIN EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German version EN ISO 13485:2016 + AC:2018 + A11:2021
Edition
2021-12
ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes
Edition
2016-03
OEVE/OENORM EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
Edition
2022-02-01
SN EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
Edition
2016-03
SN EN ISO 13485/AC
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); Corrigendum AC
Edition
2020-04
SN EN ISO 13485/A11
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); Amendment A11
Edition
2021-11
NF S99-101 ; NF EN ISO 13485:2016-04-30
Medical devices - Quality management systems - Requirements for regulatory purposes
Edition
2016-04-30
NF S99-101/A11 ; NF EN ISO 13485/A11:2021-09-08
Medical devices - Quality management systems - Requirements for regulatory purposes
Edition
2021-09-08
BS EN ISO 13485+A11
Medical devices. Quality management systems. Requirements for regulatory purposes
Edition
2016-02-29