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ISO/FDIS 18113-4 Edition
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
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  • 71.80 / copy
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Status

Final draft - Active

Origin

Technical Committee :
ISO/TC 212/WG 3 : ISO/TC 212/WG 3*

Implementation

start of the vote on the project    02/08/2021   date of ratification (dor)   
end of the vote on the project    26/10/2021   date of anouncement (doa)   
start of the vote on the final project    07/07/2022   date of publication (dop)   
end of the vote on the final project    07/09/2022   date of withdrawal (dow)   


Publication Official Journal
of the Grand-Duchy of Luxembourg
Reference

International Classification for Standards (ICS codes) :

11.100.10 : In vitro diagnostic test systems

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