- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 2, 2025
426035032DX0003PLNL-MF-000023114No 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.5 warnings recorded — scroll inside the panel to see all entries.
CW010CW007CW038CW043CW044Primary placement in Netherlands; available across 9 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jun 2, 2025 | Still on market |
| Austria | Jun 2, 2025 | Still on market |
| Belgium | Jun 2, 2025 | Still on market |
| Germany | Jun 2, 2025 | Still on market |
| Ireland | Jun 2, 2025 | Still on market |
| Luxembourg | Jun 2, 2025 | Still on market |
| Malta | Jun 2, 2025 | Still on market |
| Poland | Jun 2, 2025 | Still on market |
| XI | Jun 2, 2025 | Still on market |
(01)04260350320104
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.
W0105900101REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS