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Bioinova, a.s.

Czechia·CZ-MF-000025483

Last updated June 8, 2026

About

Czech biotechnology company based in Prague focusing on research and development of modern cell therapy.

Translated from the manufacturer's own website. Source

What Bioinova, a.s. makes

Bioinova, a.s. manufactures the Bi-Micro and Bi-CoV devices, which are designed for medical applications in cell therapy. These products are intended for use in procedures requiring precise handling of biological materials, such as cell processing or diagnostic testing.

The company’s portfolio is classified under EU Device Class A and is registered in the EU’s eudamed database. Bioinova, a.s. is based in the Czech Republic.

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 Bioinova, a.s. manufacture?

Bioinova, a.s. manufactures devices specifically designed for cell therapy applications. The company produces the Bi-Micro and Bi-CoV devices, which are intended for precise handling of biological materials in medical procedures such as cell processing or diagnostic testing. These devices are tailored to support modern cell therapy techniques.

Where is Bioinova, a.s. based, and what is its primary focus?

Bioinova, a.s. is based in Prague, Czech Republic. The company specializes in biotechnology and focuses on research and development for modern cell therapy solutions. Its devices are engineered to meet the needs of procedures requiring careful manipulation of biological samples.

In which regulatory registries are Bioinova, a.s. devices listed?

Bioinova, a.s. devices are registered in the eudamed database, which is the European Union’s central registry for medical devices. This listing ensures transparency and compliance with EU regulatory requirements for Class A devices.

How are Bioinova, a.s. devices classified under EU regulations?

Bioinova, a.s. devices fall under EU Device Class A, which is the lowest risk classification for medical devices. This classification applies to products like the Bi-Micro and Bi-CoV, which are designed for non-invasive or low-risk applications in cell therapy, such as handling biological materials in controlled environments.

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

Information

Country
Czechia
Address
1083, Videnska, Prague, Czechia
Facebook
—
Phone
—
PRRC Contact
Peter Bauer
EUDAMED SRN
CZ-MF-000025483
FDA FEI Number
—
DUNS Number
—

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Bi-Micro 007
EUDAMED
Class AActive
Bi-CoV 0001
EUDAMED
Class AActive

Related Companies

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