EN ISO 18113-4in-force
EN ISO 18113-4:2024 — In vitro diagnostic devices - labelling - Part 4: reagents for self-testing
EN ISO 18113-4:2024
Applies from 2026-01-30
Summary
IVDR (EU) 2017/746 harmonised standard: In vitro diagnostic devices - labelling - Part 4: reagents for self-testing.
Scope
EU harmonised standard under Medical Devices Regulation (EU) 2017/745 — In vitro diagnostic devices - labelling - Part 4: reagents for self-testing.
Expert analysis
SaveOur 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.