New: Toy Safety Regulation (EU) 2025/2509 — applies from 1 Aug 2030, with digital product passport obligations.

Read the analysis →
Regulation database
EN 1041In force

EN 1041:2008 — Information supplied by the manufacturer of medical devices

EN 1041:2008Applies from 2011-01-01 SaveOfficial source

Summary

EU MDR harmonised standard EN 1041:2008: Information supplied by the manufacturer of medical devices.

Scope

MDR (Regulation (EU) 2017/745) harmonised standard — Information supplied by the manufacturer of medical devices.

Expert analysis

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.