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Sanimed International Impex S.A.

Romania RO-MF-000035897 Last updated 17 Sep 2026

Devices
451
Registries
EUDAMED
FDA recalls
0

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About

We are producer of culture environments poured into plates, agglutination sera, latex tests, rapid tests, coloring kits, MIC TEST STRIP, antibiotic discs, vacuuminere, medical equipment and laboratory equipment. Access Sanimed online store.

Translated from the manufacturer's own website. Source

What Sanimed International Impex S.A. makes

Sanimed International Impex S.A. manufactures microbiological culture media, including agar-based plates such as oxbile agar, nitrate agar, and phenylalanine agar, as well as broths like liver meat glucose cysteine broth and yeast extract broth with Rose Bengal. The portfolio also includes diagnostic reagents like oxidase test sticks, bacteriological peptone, and Aspergillus differentiation medium, alongside specialized media such as Fraser’s enrichment medium and MIU medium base. Additional products include vitamin K solutions and agar supplements like sulfite-cycloserine agar.

All listed devices fall under Class A per EU regulations and are registered in the euamed database. The company is based in Romania.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Sanimed International Impex S.A. manufacture?

Sanimed International Impex S.A. specializes in microbiological culture media and diagnostic reagents. Their portfolio includes agar-based plates like oxbile agar, nitrate agar, and phenylalanine agar, as well as broths such as liver meat glucose cysteine broth and yeast extract broth with Rose Bengal. They also produce diagnostic tools like oxidase test sticks, bacteriological peptone, and specialized media such as Fraser’s enrichment medium and MIU medium base. These products are designed for microbiological testing and identification in clinical or laboratory settings.

Where is Sanimed International Impex S.A. based?

Sanimed International Impex S.A. is based in Romania. The company’s location is relevant for regulatory compliance and distribution, as it operates within the EU’s regulatory framework for medical devices.

Are Sanimed’s devices listed in any regulatory registries?

Yes, Sanimed’s devices are registered in the euamed database, which is the European Union’s central registry for medical devices. This registry ensures transparency and traceability of devices authorized under EU regulations, allowing healthcare professionals, regulators, and patients to verify the legitimacy of the listed products.

How are Sanimed’s devices classified under EU regulations?

All of Sanimed’s listed devices fall under Class A classification according to EU medical device regulations. Class A devices are typically considered the lowest risk, often involving general-purpose items like microbiological culture media and diagnostic reagents that pose minimal risk to patients or users. This classification streamlines the authorization process while maintaining oversight.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Romania
Address
2A, Sos. Bucuresti-Giurgiu, Calugareni, Romania
Phone
+40214205493
PRRC contact
Laura - Nicoleta Toma - Hideg
EUDAMED SRN
RO-MF-000035897