- Role
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- Date of registration
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EUDAMED last updated this device on Dec 1, 2025
57148828001THDK-MF-000000963No 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.Primary placement in Denmark; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | Nov 5, 2025 | Still on market |
| Belgium | Nov 5, 2025 | Still on market |
| Germany | Nov 5, 2025 | Still on market |
| Estonia | Nov 5, 2025 | Still on market |
| Spain | Nov 5, 2025 | Still on market |
| Finland | Nov 5, 2025 | Still on market |
| France | Nov 5, 2025 | Still on market |
| Ireland | Nov 5, 2025 | Still on market |
| Iceland | Nov 5, 2025 | Still on market |
| Italy | Nov 5, 2025 | Still on market |
| Netherlands | Nov 5, 2025 | Still on market |
| Norway | Nov 5, 2025 | Still on market |
| Sweden | Nov 5, 2025 | Still on market |
| XI | Nov 5, 2025 | Still on market |
(01)05714882032480
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.
Y99DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - OTHER