- Role
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- Date of registration
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EUDAMED last updated this device on Nov 28, 2025
5714882600AADK-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 15 countries total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | Apr 1, 2022 | Still on market |
| Belgium | Apr 1, 2022 | Still on market |
| Germany | Apr 1, 2022 | Still on market |
| Estonia | Feb 1, 2023 | Still on market |
| Spain | Apr 1, 2022 | Still on market |
| Finland | Apr 1, 2022 | Still on market |
| France | Apr 1, 2022 | Still on market |
| Ireland | Apr 1, 2022 | Still on market |
| Iceland | Apr 1, 2022 | Still on market |
| Italy | Apr 1, 2022 | Still on market |
| Netherlands | Apr 1, 2022 | Still on market |
| Norway | Apr 1, 2022 | Still on market |
| Sweden | Apr 1, 2022 | Still on market |
| XI | Apr 1, 2022 | Still on market |
| Austria | Apr 1, 2022 | Nov 2, 2024 |
(01)05714882031605
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