Back to all regulations
EN ISO 18113-3in-force

EN ISO 18113-3:2011 — In vitro diagnostic medical devices - Labelling - Part 3: Instruments for professional use

EN ISO 18113-3:2011

Applies from 2011-01-01

Summary

EU harmonised standard EN ISO 18113-3:2011: In vitro diagnostic medical devices - Labelling - Part 3: Instruments for professional use.

Scope

IVDR (Regulation (EU) 2017/746) / MDD harmonised standard — In vitro diagnostic medical devices - Labelling - Part 3: Instruments for professional use.

Expert analysis

Save

Our compliance experts are preparing a detailed analysis for this regulation. Check back soon.

Want this analysis for your product?

Enter your product features once — ComplyMatrix maps all applicable EU regulations, obligations and testing requirements in minutes.