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- Date of registration
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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 | Aug 25, 2011 | Still on market |
| Belgium | Aug 25, 2011 | Still on market |
| Bulgaria | Aug 25, 2011 | Still on market |
| Cyprus | Aug 25, 2011 | Still on market |
| Czechia | Aug 25, 2011 | Still on market |
| Germany | Aug 25, 2011 | Still on market |
| Denmark | Aug 25, 2011 | Still on market |
| Estonia | Aug 25, 2011 | Still on market |
| EL | Aug 25, 2011 | Still on market |
| Spain | Aug 25, 2011 | Still on market |
| Finland | Aug 25, 2011 | Still on market |
| France | Aug 25, 2011 | Still on market |
| Croatia | Aug 25, 2011 | Still on market |
| Hungary | Aug 25, 2011 | Still on market |
| Ireland | Aug 25, 2011 | Still on market |
| Iceland | Aug 25, 2011 | Still on market |
| Italy | Aug 25, 2011 | Still on market |
| Liechtenstein | Aug 25, 2011 | Still on market |
| Lithuania | Aug 25, 2011 | Still on market |
| Luxembourg | Aug 25, 2011 | Still on market |
| Malta | Aug 25, 2011 | Still on market |
| Netherlands | Aug 25, 2011 | Still on market |
| Norway | Aug 25, 2011 | Still on market |
| Poland | Aug 25, 2011 | Still on market |
| Portugal | Aug 25, 2011 | Still on market |
| Romania | Aug 25, 2011 | Still on market |
| Slovenia | Aug 25, 2011 | Still on market |
| Slovakia | Aug 25, 2011 | Still on market |
| Türkiye | Aug 25, 2011 | Still on market |
| XI | Aug 25, 2011 | Still on market |
(01)07333066005836
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