Superseded Standard
Historical

DIN EN ISO 18113-1:2013-01

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011.

Summary

This Standard defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

Notes

DIN EN ISO 18113-1 (2010-05) remains valid alongside this standard until 2014-10-31.

Technical characteristics

Publisher Deutsche Institut für Normung e.V. (DIN)
Publication Date 01/01/2013
Page Count 60
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