Every medical device placed on the Union market has a chain behind it: a manufacturer, and — when that manufacturer is established outside the EU — an authorised representative who answers for it legally. The European register holds that chain. It does not let you read it.
This site does, from whichever end you hold: 48'893 operators across 109 countries and 3'137'995 devices, snapshot of 17 August 2026.
Type the UDI-DI and you get the chain: what the device is, who makes it, and who is responsible for it in the EU.
Free, one at a time. Volume and history are the paid part.
| Manufacturer | 31'931 |
|---|---|
| Importer | 12'363 |
| Authorised representative | 2'938 |
| System/procedure pack producer | 1'661 |
| Of which listed as inactive | 1'944 |
The European register has no per-company page: everything sits behind a search form. We republish the public part in a citable form, with its source and licence. Contact details are published in the official register and are not reproduced here.