Registration number (WIID)Project No.TitleStatus
39363EN 80369-5:2016Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applicationsStandarts spēkā
69481EN ISO 13485:2016/A11:2021Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)Standarts spēkā
75110LVS EN ISO 14971:2020/A11:2022Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
12985EN ISO 15225:2000Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000)Atcelts
12981EN 1041:1998Information supplied by the manufacturer with medical devicesAtcelts
30210EN ISO 15225:2010Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO/DIS 15225:2008)Atcelts
33578EN ISO 13485:2003/AC:2009Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009)Atcelts
64861LVS CEN/TR 17223:2018Guidance on the relationship between EN ISO 13485: 2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices RegulationAtcelts
12987CR 13217:1998Nomenclature system for medical devices for the purpose of regulatory data exchange - RationaleAtcelts
24766EN 980:2008Symbols for use in the labelling of medical devicesAtcelts
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