- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Mar 25, 2026
7333066BUDI0014LRSE-MF-000014170No 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.Primary placement in Sweden; available across 30 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Jun 11, 2018 | Still on market |
| Austria | Jun 11, 2018 | Still on market |
| Belgium | Jun 11, 2018 | Still on market |
| Bulgaria | Jun 11, 2018 | Still on market |
| Cyprus | Jun 11, 2018 | Still on market |
| Czechia | Jun 11, 2018 | Still on market |
| Germany | Jun 11, 2018 | Still on market |
| Denmark | Jun 11, 2018 | Still on market |
| Estonia | Jun 11, 2018 | Still on market |
| EL | Jun 11, 2018 | Still on market |
| Spain | Jun 11, 2018 | Still on market |
| Finland | Jun 11, 2018 | Still on market |
| France | Jun 11, 2018 | Still on market |
| Croatia | Jun 11, 2018 | Still on market |
| Ireland | Jun 11, 2018 | Still on market |
| Iceland | Jun 11, 2018 | Still on market |
| Italy | Jun 11, 2018 | Still on market |
| Liechtenstein | Jun 11, 2018 | Still on market |
| Lithuania | Jun 11, 2018 | Still on market |
| Luxembourg | Jun 11, 2018 | Still on market |
| Malta | Jun 11, 2018 | Still on market |
| Netherlands | Jun 11, 2018 | Still on market |
| Norway | Jun 11, 2018 | Still on market |
| Poland | Jun 11, 2018 | Still on market |
| Portugal | Jun 11, 2018 | Still on market |
| Romania | Jun 11, 2018 | Still on market |
| Slovenia | Jun 11, 2018 | Still on market |
| Slovakia | Jun 11, 2018 | Still on market |
| Türkiye | Jun 11, 2018 | Still on market |
| XI | Jun 11, 2018 | Still on market |
(01)07333066016801
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.
W01029003BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC)