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EUDAMED last updated this device on Jun 12, 2026
84365421100992RMSALMONELLA SHIGELLA AGAR is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Reactivos para Diagnóstico. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
3843654222509184365421100992RM01-555-005(01)38436542225091
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.
W0104010101DEHYDRATED CULTURE MEDIA (DCM)No certificate specifically references this device's Basic UDI-DI.
Primary placement in Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Still on market |
ES-MF-000022523No 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.