- Role
- Country
- Date of registration
- Address
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 | Aug 1, 2018 | Still on market |
| Belgium | Aug 1, 2018 | Still on market |
| Germany | Aug 1, 2018 | Still on market |
| Estonia | Feb 1, 2023 | Still on market |
| Spain | Aug 1, 2018 | Still on market |
| Finland | Aug 1, 2018 | Still on market |
| France | Aug 1, 2018 | Still on market |
| Ireland | Aug 1, 2018 | Still on market |
| Iceland | Aug 1, 2018 | Still on market |
| Italy | Aug 1, 2018 | Still on market |
| Netherlands | Aug 1, 2018 | Still on market |
| Norway | Aug 1, 2018 | Still on market |
| Sweden | Aug 1, 2018 | Still on market |
| XI | Aug 1, 2018 | Still on market |
| Austria | Aug 1, 2018 | Nov 2, 2024 |
(01)05714882031551
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