Registration number (WIID)Project No.TitleStatus
64029EN ISO 13485:2016/AC:2016Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Atcelts
22133LVS EN ISO 13485:2003Medical devices - Quality management systems - System requirements for regulatory purposesAtcelts
21072LVS EN ISO 14971:2000/AC:2002Medical devices - Application of risk management to medical devices (ISO 14971:2000)Atcelts
24868LVS EN ISO 15225:2001 /A2:2005Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
24145LVS CEN/TR 15133:2005Nomenclature - Collective terms and codes for groups of medical devicesAtcelts
21726LVS EN ISO 15225:2001 /A1:2004Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
32012LVS EN ISO 14971:2009Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)Atcelts
24162LVS EN ISO 14971:2007Medical devices - Application of risk management to medical devicesAtcelts
32012EN ISO 14971:2009Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)Atcelts
24416LVS CEN ISO/TR 14969:2005Medical devices - Quality mangement systems - Guidance on the application of ISO 13485:2003Atcelts
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