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BIO WEST

France Last updated 21 Oct 2026

Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

About

Biowest’s vertical integration system provides origin certification and full sera traceability.

From the manufacturer's own website, in their original language. Source

What BIO WEST makes

The company produces lymphocyte separation media in two volumes: 100 mL and 500 mL, designed for isolating lymphocytes from blood samples. These products are intended for use in laboratory settings to facilitate cell processing procedures.

The portfolio consists of Class A medical devices, all of which are registered in the EU’s eudamed database. The company is headquartered in France.

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 Biowest manufacture?

Biowest manufactures lymphocyte separation media in two volumes: 100 mL and 500 mL. These products are specifically designed for isolating lymphocytes from blood samples in laboratory settings, enabling cell processing procedures. The devices are classified as Class A medical devices, indicating a low risk profile.

Where is Biowest based, and what is its primary focus?

Biowest is headquartered in France. Its primary focus is on providing lymphocyte separation media for laboratory use, ensuring quality, efficiency, and traceability in cell processing applications. The company specializes in products that assist in isolating immune cells from blood samples.

Are Biowest’s devices listed in any regulatory registries?

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

How are Biowest’s devices classified under medical device regulations?

Biowest’s devices, including the lymphocyte separation media, are classified as Class A medical devices. This classification is determined by their intended use—low-risk procedures in laboratory settings—and aligns with EU regulatory frameworks, where Class A devices require minimal regulatory oversight.

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

Information

Address
Rue de la Caille, NUAILLE, France
Phone
+33(0)241464242
PRRC contact
Jean-Philippe Hamon
EUDAMED SRN
FR-MF-000024000