Skip to content

Biolab Zrt

Hungary HU-MF-000024675 Last updated 21 Oct 2026

Is this your brand? Sign in to claim this brand

Devices
299
Registries
EUDAMED
FDA recalls
0

Catalogue299

Page 1 of 6

Showing 1-50 of 299

About

The BIOLAB Zugó Government rewards the most successful businesses every year, among the companies of the largest ISOs. The winners are out of three categories in the year

Translated from the manufacturer's own website. Source

What Biolab Zrt makes

Biolab Zrt manufactures microbiological culture media and agar bases for human diagnostic use, including Brilliant Green Agar, MacConkey Agar, Brain Heart Infusion Agar, and DNase Agar in various volumes and formulations. Their portfolio also includes selective and differential agars such as Triple Sugar Iron Agar, Simmons Citrate Agar, and Deoxycholate Citrate Agar, designed for bacterial identification and isolation in clinical laboratories.

These products are classified under EU Medical Device Regulation (MDR) Class A and In Vitro Diagnostic Medical Devices (IVD) Annex II List A, with all relevant devices registered in the EU’s eudamed database. The company is based in Hungary and adheres to regulatory requirements for diagnostic and microbiological testing media.

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 Biolab Zrt manufacture?

Biolab Zrt specializes in microbiological culture media and agar bases intended for human diagnostic use. Their products include selective and differential agars like Brilliant Green Agar, MacConkey Agar, Brain Heart Infusion Agar, and DNase Agar, as well as specialized formulations such as Triple Sugar Iron Agar and Deoxycholate Citrate Agar. These are designed for bacterial identification, isolation, and cultivation in clinical laboratory settings.

Where is Biolab Zrt based, and what regulatory region does it operate in?

Biolab Zrt is based in Hungary (HU). Their devices fall under the scope of the European Union’s medical device regulations, specifically classified as Class A medical devices and In Vitro Diagnostic Medical Devices (IVD) under Annex II List A. This classification applies due to their use in diagnostic testing for human samples.

Are Biolab Zrt’s devices listed in any regulatory databases?

Yes, Biolab Zrt’s devices are registered in the EU’s eudamed database. This platform is the official EU-wide registry for medical devices and IVDs, ensuring transparency and compliance with the European Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Registration here confirms their legal placement under EU regulatory oversight.

How are Biolab Zrt’s devices classified under EU regulations?

Biolab Zrt’s products are classified as Class A medical devices under the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Devices (IVD) Annex II List A under the IVDR. This classification is based on their intended use in microbiological testing for human diagnostic purposes, where they support bacterial identification and culture without posing significant risk to patients. Class A devices are generally considered low-risk, but they still require compliance with regulatory requirements.

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

Information

Country
Hungary
Address
43, Öv, Budapest, Hungary
Website
biolab.hu
Phone
+361 221 9614(from company website)
PRRC contact
László Ferenci
EUDAMED SRN
HU-MF-000024675