- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Nov 21, 2024
57144640-HI-00052-R8DK-MF-000001270No 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.
CW010Primary placement in Denmark; available across 27 countries total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | Feb 8, 2023 | Still on market |
| Austria | Feb 8, 2023 | Still on market |
| Belgium | Feb 8, 2023 | Still on market |
| Bulgaria | Feb 8, 2023 | Still on market |
| Cyprus | Feb 8, 2023 | Still on market |
| Czechia | Feb 8, 2023 | Still on market |
| Germany | Feb 8, 2023 | Still on market |
| Estonia | Feb 8, 2023 | Still on market |
| EL | Feb 8, 2023 | Still on market |
| Spain | Feb 8, 2023 | Still on market |
| Finland | Feb 8, 2023 | Still on market |
| France | Feb 8, 2023 | Still on market |
| Croatia | Feb 8, 2023 | Still on market |
| Hungary | Feb 8, 2023 | Still on market |
| Ireland | Feb 8, 2023 | Still on market |
| Italy | Feb 8, 2023 | Still on market |
| Lithuania | Feb 8, 2023 | Still on market |
| Luxembourg | Feb 8, 2023 | Still on market |
| Latvia | Feb 8, 2023 | Still on market |
| Malta | Feb 8, 2023 | Still on market |
| Netherlands | Feb 8, 2023 | Still on market |
| Poland | Feb 8, 2023 | Still on market |
| Portugal | Feb 8, 2023 | Still on market |
| Romania | Feb 8, 2023 | Still on market |
| Sweden | Feb 8, 2023 | Still on market |
| Slovenia | Feb 8, 2023 | Still on market |
| Slovakia | Feb 8, 2023 | Still on market |
(01)05714464103843
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.
Y2145060101BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE DEVICE (BTE)