Compliance
We work within European standards, so you don't carry the paperwork burden.
Every device in our network is sourced from suppliers who provide CE certification and full compliance documentation. We do not facilitate any transaction that cannot be accompanied by the required paperwork.
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CE marking & EU MDR 2017/745
CE marking is a manufacturer’s declaration that a medical device meets the health, safety, and environmental requirements of European Union law. For medical equipment, this is governed by EU MDR 2017/745, the regulation that sets the rules for design, manufacturing, and post-market surveillance.
MedevEur works exclusively with CE-certified sources. Refurbishers in our network follow procedures that maintain a device’s compliance status, and the documentation travels with the equipment so buyers and regulators can verify it at every stage.
What ships with every device
- CE certificate
- Decontamination certificate
- Technical inspection report
- Service & calibration records
- Packing list & export invoice
- Condition grade report
Documentation is verified before every order is confirmed.
GDPR & data protection
MedevEur operates under EU jurisdiction in full compliance with GDPR. Personal data submitted through this website is used solely to respond to your inquiry and is never shared with third parties.