Who is responsible for this medical device in Europe?

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.

You have a barcode from a box

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.

You have a market to measure, or a watch to keep

Pro access — looking for more than one? Match your supplier list against SRNs, monitor entries and exits from the register, bulk search. And if it is the full dataset you need, see Data.

What the register contains

Manufacturer31'931
Importer12'363
Authorised representative2'938
System/procedure pack producer1'661
Of which listed as inactive1'944

By country

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.

The full dataset →