- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 30, 2026
40997970006011000000000FK0409979701972840997970006011000000000FKKA2136.3840(01)04099797019728
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.
P01020180DENTAL IMPLANTS - ACCESSORIES4 warnings recorded — scroll inside the panel to see all entries.
CW010CW011CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 18 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Apr 30, 2026 | Still on market |
| Austria | Apr 30, 2026 | Still on market |
| Belgium | Apr 30, 2026 | Still on market |
| Bulgaria | Apr 30, 2026 | Still on market |
| Czechia | Apr 30, 2026 | Still on market |
| Denmark | Apr 30, 2026 | Still on market |
| Spain | Apr 30, 2026 | Still on market |
| France | Apr 30, 2026 | Still on market |
| Hungary | Apr 30, 2026 | Still on market |
| Ireland | Apr 30, 2026 | Still on market |
| Italy | Apr 30, 2026 | Still on market |
| Liechtenstein | Apr 30, 2026 | Still on market |
| Luxembourg | Apr 30, 2026 | Still on market |
| Netherlands | Apr 30, 2026 | Still on market |
| Poland | Apr 30, 2026 | Still on market |
| Portugal | Apr 30, 2026 | Still on market |
| Slovakia | Apr 30, 2026 | Still on market |
| Türkiye | Apr 30, 2026 | Still on market |
DE-MF-000006230No 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.