- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Nov 12, 2025
594054037MEDIUMUELLER5C6MEDIU MUELLER HINTON (MUELLER HINTON AGAR) is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Sanimed International Impex S.A.. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0594054037449810778(01)05940540374498
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0104010306CULTURE MEDIA IN BOTTLESRO-MF-000035897No 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.The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Romania; available across 1 country total.
Placed on the market in Romania; per-country availability dates not published.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
594054037MEDIUMUELLER34L6On the marketMEDIU MUELLER HINTON (MUELLER HINTON AGAR)594054037MEDIUMUELLER6C8On the marketMEDIU MUELLER HINTON (MUELLER HINTON AGAR)594054037MEDIUMUELLER4C4On the marketMEDIU MUELLER KAUFFMAN (MUELER KAUFFMAN BROTH)594054037MEDIUMUELLER3C2On the marketMEDIU MUELLER KAUFFMAN (MUELER KAUFFMAN BROTH)594054037MEDIUMUELLER2BYOn the marketMEDIU MUELLER KAUFFMAN (MUELER KAUFFMAN BROTH)594054037MEDIUMUELLER1BWOn the market