- Role
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- Date of registration
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EUDAMED last updated this device on May 2, 2025
57071313-PA-00003-KUDK-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 | Jun 19, 2020 | Still on market |
| Austria | Jun 19, 2020 | Still on market |
| Belgium | Jun 19, 2020 | Still on market |
| Bulgaria | Jun 19, 2020 | Still on market |
| Cyprus | Jun 19, 2020 | Still on market |
| Czechia | Jun 19, 2020 | Still on market |
| Germany | Jun 19, 2020 | Still on market |
| Estonia | Jun 19, 2020 | Still on market |
| EL | Jun 19, 2020 | Still on market |
| Spain | Jun 19, 2020 | Still on market |
| Finland | Jun 19, 2020 | Still on market |
| France | Jun 19, 2020 | Still on market |
| Croatia | Jun 19, 2020 | Still on market |
| Hungary | Jun 19, 2020 | Still on market |
| Ireland | Jun 19, 2020 | Still on market |
| Italy | Jun 19, 2020 | Still on market |
| Lithuania | Jun 19, 2020 | Still on market |
| Luxembourg | Jun 19, 2020 | Still on market |
| Latvia | Jun 19, 2020 | Still on market |
| Malta | Jun 19, 2020 | Still on market |
| Netherlands | Jun 19, 2020 | Still on market |
| Poland | Jun 19, 2020 | Still on market |
| Portugal | Jun 19, 2020 | Still on market |
| Romania | Jun 19, 2020 | Still on market |
| Sweden | Jun 19, 2020 | Still on market |
| Slovenia | Jun 19, 2020 | Still on market |
| Slovakia | Jun 19, 2020 | Still on market |
(01)05707131250827
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.
Y214580HEARING AIDS OR HEARING DEVICES - ACCESSORIES