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EUDAMED last updated this device on May 25, 2026
69207567KXXWTXQ00018W6692075671805869207567KXXWTXQ00018WHD-16H-001 (01)66920756718058
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.
F01060203DIALYSERS - UFC = 18 - 35 ml/h/mmHg, SYNTHETIC MEMBRANES3 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Hungary; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary placement | Jan 1, 2025 | Dec 31, 2050 |
| Austria | Jan 1, 2025 | Dec 31, 2050 |
| Belgium | Jan 1, 2025 | Dec 31, 2050 |
| Bulgaria | Jan 1, 2025 | Dec 31, 2050 |
| Cyprus | Jan 1, 2025 | Dec 31, 2050 |
| Czechia | Jan 1, 2025 | Dec 31, 2050 |
| Germany | Jan 1, 2025 | Dec 31, 2050 |
| Denmark | Jan 1, 2025 | Dec 31, 2050 |
| Estonia | Jan 1, 2025 | Dec 31, 2050 |
| EL | Jan 1, 2025 | Dec 31, 2050 |
| Spain | Jan 1, 2025 | Dec 31, 2050 |
| Finland | Jan 1, 2025 | Dec 31, 2050 |
| France | Jan 1, 2025 | Dec 31, 2050 |
| Croatia | Jan 1, 2025 | Dec 31, 2050 |
| Ireland | Jan 1, 2025 | Dec 31, 2050 |
| Iceland | Jan 1, 2025 | Dec 31, 2050 |
| Italy | Jan 1, 2025 | Dec 31, 2050 |
| Liechtenstein | Jan 1, 2025 | Dec 31, 2050 |
| Lithuania | Jan 1, 2025 | Dec 31, 2050 |
| Luxembourg | Jan 1, 2025 | Dec 31, 2050 |
| Latvia | Jan 1, 2025 | Dec 31, 2050 |
| Malta | Jan 1, 2025 | Dec 31, 2050 |
| Netherlands | Jan 1, 2025 | Dec 31, 2050 |
| Norway | Jan 1, 2025 | Dec 31, 2050 |
| Poland | Jan 1, 2025 | Dec 31, 2050 |
| Portugal | Jan 1, 2025 | Dec 31, 2050 |
| Romania | Jan 1, 2025 | Dec 31, 2050 |
| Sweden | Jan 1, 2025 | Dec 31, 2050 |
| Slovenia | Jan 1, 2025 | Dec 31, 2050 |
| Slovakia | Jan 1, 2025 | Dec 31, 2050 |
| Türkiye | Jan 1, 2025 | Dec 31, 2050 |
| XI | Jan 1, 2025 | Dec 31, 2050 |
CN-MF-000006019No 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.69207567KXXWTXQ00018WOn the marketHollow fiber hemodialyzer low-flux69207567KXXWTXQ00028YOn the marketBlood collection needles for single use69207567CXZ001RJOn the marketBlood collection needles for single use69207567CXZ001RJOn the marketBlood collection needles for single use69207567CXZ001RJOn the market