Registration number (WIID)Project No.TitleStatus
30210LVS EN ISO 15225:2010Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2010)Atcelts
24868LVS EN ISO 15225:2001 /A2:2005Nomenclature - 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
12985LVS EN ISO 15225:2001Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchangeAtcelts
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
68559LVS EN ISO 15223-1:2021Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)Standarts spēkā
59550LVS EN ISO 15223-1:2017Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2016-12-15)Atcelts
31133LVS EN ISO 15223-1:2012Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2012) 
75110LVS EN ISO 14971:2020/A11:2022Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
63920LVS EN ISO 14971:2020Medical devices - Application of risk management to medical devices (ISO 14971:2019)Standarts spēkā
Displaying 31-40 of 145 results.