- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 12, 2023
3663999RWS01A5sterEOS is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by EOS imaging. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
036639990000473663999RWS01A5sterEOS(01)03663999000047
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z11069005DIAGNOSTIC IMAGING WORKSTATIONSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Dec 12, 2022 | Still on market |
| Austria | Dec 12, 2022 | Still on market |
| Belgium | Dec 12, 2022 | Still on market |
| Czechia | Dec 12, 2022 | Still on market |
| Germany | Dec 12, 2022 | Still on market |
| Denmark | Dec 12, 2022 | Still on market |
| Spain | Dec 12, 2022 | Still on market |
| Finland | Dec 12, 2022 | Still on market |
| Hungary | Dec 12, 2022 | Still on market |
| Italy | Dec 12, 2022 | Still on market |
| Netherlands | Dec 12, 2022 | Still on market |
| Poland | Dec 12, 2022 | Still on market |
| Portugal | Dec 12, 2022 | Still on market |
| Romania | Dec 12, 2022 | Still on market |
| Sweden | Dec 12, 2022 | Still on market |
FR-MF-000000502No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.