- Role
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- Date of registration
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EUDAMED last updated this device on Sep 5, 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 | Sep 5, 2025 | Still on market |
| Austria | Sep 5, 2025 | Still on market |
| Belgium | Sep 5, 2025 | Still on market |
| Germany | Sep 5, 2025 | Still on market |
| Ireland | Sep 5, 2025 | Still on market |
| Luxembourg | Sep 5, 2025 | Still on market |
| Malta | Sep 5, 2025 | Still on market |
| Poland | Sep 5, 2025 | Still on market |
| XI | Sep 5, 2025 | Still on market |
(01)04260350320135
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