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Overview ISO 18113-1:2022 - "In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements" defines the core concep…
Overview ISO 18113-4:2022 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing - specifies the required…
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-…
Overview ISO 18113-2:2022 - "In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use" specifies labellin…
Overview ISO 18113-3:2022 specifies the labelling and information requirements for in vitro diagnostic (IVD) instruments intended for professional use. It defines what manufacturers must supply with…
1 Scope This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self-testing. This part of ISO 18113 also applies to information supplied by the…
What is ISO 18113-3 - In vitro diagnostic instruments for professional use about? ISO 18113 is a European standard that discusses information supplied by the manufacturer regarding In vitro diagnosti…
1 Scope This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices . This part of…
1 Scope This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use. This part of ISO 18113 also applies to information supplied by…
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…