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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 | May 7, 2008 | Still on market |
| Belgium | May 7, 2008 | Still on market |
| Bulgaria | May 7, 2008 | Still on market |
| Cyprus | May 7, 2008 | Still on market |
| Czechia | May 7, 2008 | Still on market |
| Germany | May 7, 2008 | Still on market |
| Denmark | May 7, 2008 | Still on market |
| Estonia | May 7, 2008 | Still on market |
| EL | May 7, 2008 | Still on market |
| Spain | May 7, 2008 | Still on market |
| Finland | May 7, 2008 | Still on market |
| France | May 7, 2008 | Still on market |
| Croatia | May 7, 2008 | Still on market |
| Hungary | May 7, 2008 | Still on market |
| Ireland | May 7, 2008 | Still on market |
| Iceland | May 7, 2008 | Still on market |
| Italy | May 7, 2008 | Still on market |
| Liechtenstein | May 7, 2008 | Still on market |
| Lithuania | May 7, 2008 | Still on market |
| Luxembourg | May 7, 2008 | Still on market |
| Malta | May 7, 2008 | Still on market |
| Netherlands | May 7, 2008 | Still on market |
| Norway | May 7, 2008 | Still on market |
| Poland | May 7, 2008 | Still on market |
| Portugal | May 7, 2008 | Still on market |
| Romania | May 7, 2008 | Still on market |
| Slovenia | May 7, 2008 | Still on market |
| Slovakia | May 7, 2008 | Still on market |
| Türkiye | May 7, 2008 | Still on market |
| XI | May 7, 2008 | Still on market |
(01)07333066010519
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