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EUDAMED last updated this device on May 26, 2026
4060139000072PDE-MF-000006975No 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.
CW999Primary placement in Germany; available across 28 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jul 15, 2019 | Still on market |
| Austria | Jul 15, 2019 | Still on market |
| Belgium | Jul 15, 2019 | Still on market |
| Cyprus | Jul 15, 2019 | Still on market |
| Czechia | Jul 15, 2019 | Still on market |
| Denmark | Jul 15, 2019 | Still on market |
| Estonia | Jul 15, 2019 | Still on market |
| EL | Jul 15, 2019 | Still on market |
| Spain | Jul 15, 2019 | Still on market |
| Finland | Jul 15, 2019 | Still on market |
| France | Jul 15, 2019 | Still on market |
| Hungary | Jul 15, 2019 | Still on market |
| Ireland | Jul 15, 2019 | Still on market |
| Italy | Jul 15, 2019 | Still on market |
| Lithuania | Jul 15, 2019 | Still on market |
| Luxembourg | Jul 15, 2019 | Still on market |
| Latvia | Jul 15, 2019 | Still on market |
| Malta | Jul 15, 2019 | Still on market |
| Netherlands | Jul 15, 2019 | Still on market |
| Norway | Jul 15, 2019 | Still on market |
| Poland | Jul 15, 2019 | Still on market |
| Portugal | Jul 15, 2019 | Still on market |
| Romania | Jul 15, 2019 | Still on market |
| Sweden | Jul 15, 2019 | Still on market |
| Slovenia | Jul 15, 2019 | Still on market |
| Slovakia | Jul 15, 2019 | Still on market |
| Türkiye | Jul 15, 2019 | Still on market |
| XI | Jul 15, 2019 | Still on market |
(01)04060139400207
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.
R0301020302HIGH FLOW THERAPY NASAL CANNULAS (HFNC)