Поиск

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro…

Overview SIST EN ISO 18113-5:2024 specifies the requirements for information supplied by manufacturers of in vitro diagnostic (IVD) instruments intended for self-testing. Published by the European Co…

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro…

Overview EN ISO 18113-5:2024 specifies the requirements for information supplied by manufacturers of in vitro diagnostic (IVD) instruments intended for self-testing. Published by the European Committ…

Tracked Changes. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). I…

In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) - In vitro diagnost…

1 Scope This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for self-testing. This part of ISO 18113 also applies to apparatus and equipment…

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro…

Overview ISO 18113-5:2022 - part of the ISO 18113 series - specifies requirements for information supplied by the manufacturer (labelling) for in vitro diagnostic (IVD) instruments intended for self-…

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro…

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling). Part 5: In vitro…