Registration number (WIID)Project No.TitleStatus
77026prEN ISO 18250-8Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 8: Citrate-based anticoagulant solution for apheresis applicationsIzstrādē
32600EN 15986:2011Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalatesIzstrādē
64227EN ISO 80369-3:2016/prA2Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 2 (ISO 80369-3:2016/DAmd 2:2017)Izstrādē
79260prEN ISO 20417Medical devices - Information to be supplied by the manufacturer (ISO/DIS 20417:2024)Izstrādē
64226EN ISO 80369-3:2016/prA1Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/DAmd 1:2017)Izstrādē
81836prCEN ISO/TS 23485Medical Devices -- Quality management systems -- Guideline for the application of ISO 13485:2016Izstrādē
24165prEN ISO 14971-BMedical devices -- Application of risk management to medical devices -- Part B: In vitro diagnostic medical devicesIzstrādē
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
12981EN 1041:1998Information supplied by the manufacturer with medical devicesAtcelts
12985EN ISO 15225:2000Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000)Atcelts
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