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General requirements for in vitro diagnostic medical devices for self-testing Ingestion-build-59651 For an organization to function

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Description

For an organization to function effectively it has to identify and manage numerous linked activities

within budget and to customer specification

Inspection and testing

Annex A (informative) Iris image capture

For higher pressures

General requirements for in vitro diagnostic medical devices for self-testing Ingestion-build-59651 For an organization to functionBS EN 13532: 2002 specifies general requirements for in vitro diagnostic medical devices (IVD MDs) for self testing in order to ensure that IVD MDs for self testing are safe and suitable for the purposes as specified by the manufacturer. This European standard does not address medical aspects of IVD MDs for self testing.

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