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About This Item
Document History
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DIN EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) (includes Corrigendum :2018)- Most Recent
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DIN EN ISO 13485/A1 - DRAFT
Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German and English version EN ISO 13485:2016/prA1:2019- Historical Version
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DIN EN ISO 13485 Corrigendum 1
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) , Corrigendum to DIN EN ISO 13485:2016-08- Historical Version
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DIN EN ISO 13485
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Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)- Historical Version
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DIN EN ISO 13485 - DRAFT
Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO/DIS 13485:2015); German and English version prEN ISO 13485:2015- Historical Version
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DIN EN ISO 13485 - DRAFT
Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO/DIS 13485:2014); German version prEN ISO 13485:2014- Historical Version
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DIN EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 + Cor. 1:2009) (includes Corrigendum :2012)- Historical Version
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DIN EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 + Cor. 1:2009) (includes Corrigendum AC:2009)- Historical Version
-
DIN EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) (includes Corrigendum AC:2007)- Historical Version