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EUDAMED last updated this device on Apr 14, 2026
038290YDBYCJUGF2446093 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by BD Kiestra B.V.. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
00382904460938038290YDBYCJUGF2446093(01)00382904460938
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.
W02039080VARIOUS MICROBIOLOGY INSTRUMENTS - HARDWARE ACCESSORIES17 warnings recorded — scroll inside the panel to see all entries.
CW010CW011CW007CW999CW999CW999CW999CW999CW999CW999CW999CW999CW999CW999CW999CW999CW999No certificate specifically references this device's Basic UDI-DI.
Primary placement in Belgium; available across 6 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| Netherlands | Still on market | |
| Norway | Still on market | |
| Poland | Still on market |
NL-MF-000018863No 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.