Udi/mdr Training
Master EU-MDR and UDI for medical devices used in healthcare. Learn labeling, risk classification, IFU, UDI/EUDAMED data, and post-market updates so your devices stay compliant, traceable, and safe for patients and clinicians.

4 to 360 hours of flexible workload
valid certificate in your country
What Will I Learn?
Udi/mdr Training gives you a focused, practical guide to EU-MDR labelling and UDI for complex devices such as reusable, Bluetooth-enabled infusion pumps. Learn legal requirements, risk classification, mandatory label and packaging content, IFU and electronic information rules, usability and risk controls, plus UDI/EUDAMED data and workflows so your documentation is compliant, traceable, and inspection-ready.
Elevify Differentials
Develop Skills
- EU-MDR labeling mastery: apply Annex I, II, III rules to real device labels.
- UDI and EUDAMED skills: build compliant UDI-DI/PI data and register devices fast.
- IFU and e-IFU writing: create clear, localized, Annex I–compliant instructions.
- Risk-based labeling: design warnings, symbols and IFU content to reduce misuse.
- Bluetooth device compliance: align software, connectivity and cybersecurity labeling.
Suggested Summary
Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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