In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic reagents for self-testing Ingestion-build-48183 This International Standard establishes a

This International Standard establishes a terminology for

PAS 402:2013 supersedes PAS 402:2009

These professionals need to have sufficient experience

BS EN 13920-16 specifies characteristics

In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic reagents for self-testing Ingestion-build-48183 This International Standard establishes a1 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 manufacturer with calibrators and control materials intended for use with IVD medical devices for self testing. This part of ISO 18113 can also be applied to accessories. This part of ISO 18113 applies to the labels for outer and immediate containers and