- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Mar 25, 2026
7333066BUDI0039M9SE-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.1 warning recorded — scroll inside the panel to see all entries.
CW009Primary placement in Sweden; available across 13 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Still on market | |
| Austria | Sep 13, 2005 | Still on market |
| Cyprus | Sep 13, 2005 | Still on market |
| Germany | Sep 13, 2005 | Still on market |
| Denmark | Sep 13, 2005 | Still on market |
| Finland | Sep 13, 2005 | Still on market |
| France | Sep 13, 2005 | Still on market |
| Ireland | Sep 13, 2005 | Still on market |
| Iceland | Sep 13, 2005 | Still on market |
| Liechtenstein | Sep 13, 2005 | Still on market |
| Luxembourg | Sep 13, 2005 | Still on market |
| Malta | Sep 13, 2005 | Still on market |
| Norway | Sep 13, 2005 | Still on market |
(01)07333066017679
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.
W01029003BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC)