Registration number (WIID)Project No.TitleStatus
77231LVS EN ISO 15223-1:2021/A1:2025Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific (ISO 15223 1:2021/Amd 1:2025)Standarts spēkā
12985LVS EN ISO 15225:2001Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
21726LVS EN ISO 15225:2001 /A1:2004Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
24868LVS EN ISO 15225:2001 /A2:2005Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
30210LVS EN ISO 15225:2010Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2010)Atcelts
39825LVS EN ISO 15225:2016Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016)Atcelts
67368LVS EN ISO 20417:2021Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021,Ccorrected version 2021-12)Standarts spēkā
79260LVS EN ISO 20417:2026Medical devices - Information to be supplied by the manufacturer (ISO 20417:2026) 
31251LVS EN ISO 80369-1:2011Small bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2010)Atcelts
40585LVS EN ISO 80369-1:2019Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2018)Standarts spēkā
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