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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 | Nov 2, 2009 | Still on market |
| Belgium | Nov 2, 2009 | Still on market |
| Bulgaria | Nov 2, 2009 | Still on market |
| Cyprus | Nov 2, 2009 | Still on market |
| Czechia | Nov 2, 2009 | Still on market |
| Germany | Nov 2, 2009 | Still on market |
| Denmark | Nov 2, 2009 | Still on market |
| Estonia | Nov 2, 2009 | Still on market |
| EL | Nov 2, 2009 | Still on market |
| Spain | Nov 2, 2009 | Still on market |
| Finland | Nov 2, 2009 | Still on market |
| France | Nov 2, 2009 | Still on market |
| Croatia | Nov 2, 2009 | Still on market |
| Hungary | Nov 2, 2009 | Still on market |
| Ireland | Nov 2, 2009 | Still on market |
| Iceland | Nov 2, 2009 | Still on market |
| Italy | Nov 2, 2009 | Still on market |
| Liechtenstein | Nov 2, 2009 | Still on market |
| Lithuania | Nov 2, 2009 | Still on market |
| Luxembourg | Nov 2, 2009 | Still on market |
| Malta | Nov 2, 2009 | Still on market |
| Netherlands | Nov 2, 2009 | Still on market |
| Norway | Nov 2, 2009 | Still on market |
| Poland | Nov 2, 2009 | Still on market |
| Portugal | Nov 2, 2009 | Still on market |
| Romania | Nov 2, 2009 | Still on market |
| Slovenia | Nov 2, 2009 | Still on market |
| Slovakia | Nov 2, 2009 | Still on market |
| Türkiye | Nov 2, 2009 | Still on market |
| XI | Nov 2, 2009 | Still on market |
(01)07333066005676
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