- Role
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- Date of registration
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EUDAMED last updated this device on Dec 22, 2023
805750258LINEATRACHEO5DIT-MF-0000296782 warnings recorded — scroll inside the panel to see all entries.
CW162CW275Primary placement in Italy; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Bulgaria | Still on market | |
| Cyprus | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| Denmark | Still on market | |
| Estonia | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| Finland | Still on market | |
| France | Still on market | |
| Croatia | Still on market | |
| Hungary | Still on market | |
| Ireland | Still on market | |
| Iceland | Still on market | |
| Liechtenstein | Still on market | |
| Lithuania | Still on market | |
| Luxembourg | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Norway | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Romania | Still on market | |
| Sweden | Still on market | |
| Slovenia | Still on market | |
| Slovakia | Still on market | |
| Türkiye | Still on market | |
| XI | Still on market |
(01)08057502580006
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.
R010599TRACHEOSTOMY AND LARYNGECTOMY CANNULAS - OTHER805750258COLLAREGORG4KOn the market908997758 805750258ENTEROCLISMAVI4COn the marketFARMAWALK ELBOW CRUTCH W/O SHOCK ABSORBER 1 PAIR805750258CANADESIQ4On the marketFARMAWALK ELBOW CRUTCH W/O SHOCK ABSORBER 1PC805750258CANADESIQ4On the marketHot water bottle Plus BS Standard805750258BORSAACALDABSZDOn the marketNo 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.