Registration number (WIID)Project No.TitleStatus
33753ISO/TS 19218:2005Medical devices — Coding structure for adverse event type and causeAtcelts
58085ISO/TS 19218-1:2011/Amd 1:2013Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes — Amendment 1Atcelts
55589ISO/TS 19218-1:2011Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codesAtcelts
69336ISO/TS 11633-1:2019Health informatics — Information security management for remote maintenance of medical devices and medical information systems — Part 1: Requirements and risk analysisStandarts spēkā
60044ISO/TR 80002-2:2017Medical device software — Part 2: Validation of software for medical device quality systemsStandarts spēkā
74437ISO/TR 24971:2020Medical devices — Guidance on the application of ISO 14971Standarts spēkā
59587ISO/TR 24971:2013Medical devices — Guidance on the application of ISO 14971Atcelts
67942ISO/TR 20416:2020Medical devices — Post-market surveillance for manufacturersStandarts spēkā
38401ISO/TR 16142:2006Medical devices — Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devicesAtcelts
30163ISO/TR 16142:1999Medical devices — Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devicesAtcelts
Displaying 11-20 of 114 results.