- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jan 22, 2026
871865721TPU-TAD7WNL-MF-000022827No 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.4 warnings recorded — scroll inside the panel to see all entries.
CW009CW001CW007CW018Primary placement in Netherlands; available across 18 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jan 1, 2026 | Still on market |
| Austria | Jan 1, 2026 | Still on market |
| Belgium | Jan 1, 2026 | Still on market |
| Germany | Jan 1, 2026 | Still on market |
| Denmark | Jan 1, 2026 | Still on market |
| EL | Jan 1, 2026 | Still on market |
| Finland | Jan 1, 2026 | Still on market |
| Croatia | Jan 1, 2026 | Still on market |
| Ireland | Jan 1, 2026 | Still on market |
| Italy | Jan 1, 2026 | Still on market |
| Malta | Jan 1, 2026 | Still on market |
| Norway | Jan 1, 2026 | Still on market |
| Poland | Jan 1, 2026 | Still on market |
| Portugal | Jan 1, 2026 | Still on market |
| Romania | Jan 1, 2026 | Still on market |
| Sweden | Jan 1, 2026 | Still on market |
| Slovenia | Jan 1, 2026 | Still on market |
| XI | Jan 1, 2026 | Still on market |
(01)08718657214344
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.
U01010501NELATON CATHETERS, SELF-LUBRICATING