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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 | Sep 24, 2008 | Still on market |
| Belgium | Sep 24, 2008 | Still on market |
| Bulgaria | Sep 24, 2008 | Still on market |
| Cyprus | Sep 24, 2008 | Still on market |
| Czechia | Sep 24, 2008 | Still on market |
| Germany | Sep 24, 2008 | Still on market |
| Denmark | Sep 24, 2008 | Still on market |
| Estonia | Sep 24, 2008 | Still on market |
| EL | Sep 24, 2008 | Still on market |
| Spain | Sep 24, 2008 | Still on market |
| Finland | Sep 24, 2008 | Still on market |
| France | Sep 24, 2008 | Still on market |
| Croatia | Sep 24, 2008 | Still on market |
| Hungary | Sep 24, 2008 | Still on market |
| Ireland | Sep 24, 2008 | Still on market |
| Iceland | Sep 24, 2008 | Still on market |
| Italy | Sep 24, 2008 | Still on market |
| Liechtenstein | Sep 24, 2008 | Still on market |
| Lithuania | Sep 24, 2008 | Still on market |
| Luxembourg | Sep 24, 2008 | Still on market |
| Malta | Sep 24, 2008 | Still on market |
| Netherlands | Sep 24, 2008 | Still on market |
| Norway | Sep 24, 2008 | Still on market |
| Poland | Sep 24, 2008 | Still on market |
| Portugal | Sep 24, 2008 | Still on market |
| Romania | Sep 24, 2008 | Still on market |
| Slovenia | Sep 24, 2008 | Still on market |
| Slovakia | Sep 24, 2008 | Still on market |
| Türkiye | Sep 24, 2008 | Still on market |
| XI | Sep 24, 2008 | Still on market |
(01)07333066005614
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.
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