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EUDAMED last updated this device on Mar 25, 2026
7333066BUDI0017LXSE-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 31 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Still on market | |
| Austria | Dec 1, 2003 | Still on market |
| Belgium | Dec 1, 2003 | Still on market |
| Bulgaria | Dec 1, 2003 | Still on market |
| Cyprus | Dec 1, 2003 | Still on market |
| Czechia | Dec 1, 2003 | Still on market |
| Germany | Dec 1, 2003 | Still on market |
| Denmark | Dec 1, 2003 | Still on market |
| Estonia | Dec 1, 2003 | Still on market |
| EL | Dec 1, 2003 | Still on market |
| Spain | Dec 1, 2003 | Still on market |
| Finland | Dec 1, 2003 | Still on market |
| France | Dec 1, 2003 | Still on market |
| Croatia | Dec 1, 2003 | Still on market |
| Hungary | Dec 1, 2003 | Still on market |
| Ireland | Dec 1, 2003 | Still on market |
| Iceland | Dec 1, 2003 | Still on market |
| Italy | Dec 1, 2003 | Still on market |
| Liechtenstein | Dec 1, 2003 | Still on market |
| Lithuania | Dec 1, 2003 | Still on market |
| Luxembourg | Dec 1, 2003 | Still on market |
| Malta | Dec 1, 2003 | Still on market |
| Netherlands | Dec 1, 2003 | Still on market |
| Norway | Dec 1, 2003 | Still on market |
| Poland | Dec 1, 2003 | Still on market |
| Portugal | Dec 1, 2003 | Still on market |
| Romania | Dec 1, 2003 | Still on market |
| Slovenia | Dec 1, 2003 | Still on market |
| Slovakia | Dec 1, 2003 | Still on market |
| Türkiye | Dec 1, 2003 | Still on market |
| XI | Dec 1, 2003 | Still on market |
(01)07333066006130
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.
W01020202IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT