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EUDAMED last updated this device on Mar 13, 2025
590575374SAL001E4Salmonella Antiserum O:13/O:G - 1ml is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Zakład Badawczo-Wdrożeniowy Ośrodka Salmonella "IMMUNOLAB" Sp. z o. o.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05905753740751590575374SAL001E4SS032(01)05905753740751
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.
W0104080301SEROTYPING (E.COLI, SALMONELLA, SHIGELLA, ETC)1 warning recorded — scroll inside the panel to see all entries.
CW267No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 1 country total.
Placed on the market in Poland; per-country availability dates not published.
PL-MF-000042563No 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.590575374PS006FAOn the marketRabbit coagulase plasma (lyophilized) - 2ml590575374OSO002KDOn the marketRabbit coagulase plasma (lyophilized) - 5ml590575374OSO002KDOn the marketSalmonella Antiserum H:1 - 1ml590575374SAL001E4On the marketSalmonella Antiserum H:1 - 2ml590575374SAL001E4On the market