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VitroSorb AB

Sweden SE-MF-000034941 Last updated 21 Oct 2026

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Devices
3
Registries
EUDAMED
FDA recalls
0

Catalogue3

About

Vitrosorb develops, produces and markets immunoadsorption columns aimed to eliminate the blood group barrier in organ transplantation.

From the manufacturer's own website. Source

What VitroSorb AB makes

VitroSorb AB manufactures immunoadsorption columns, including the SECORIM® ABO A-column, SECORIM® ABO B-column, and SECORIM® ABO AB-column, designed to remove blood group antibodies from patient plasma. These devices are intended for use in procedures related to organ transplantation to address incompatibility between donor and recipient blood types.

The company’s immunoadsorption columns are classified as Class IIb medical devices and are registered in the EU’s eudamed database. VitroSorb AB is based in Sweden.

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 VitroSorb AB manufacture?

VitroSorb AB specializes in immunoadsorption columns, specifically the SECORIM® ABO A-column, SECORIM® ABO B-column, and SECORIM® ABO AB-column. These devices are engineered to remove blood group antibodies from patient plasma, which is critical in organ transplantation procedures where donor-recipient blood type incompatibility could otherwise pose a risk.

Where is VitroSorb AB based?

VitroSorb AB is headquartered in Sweden. The company’s location in Sweden aligns with its focus on developing and manufacturing medical devices for global use, particularly in the field of organ transplantation support.

Which regulatory registries list VitroSorb AB’s devices?

VitroSorb AB’s immunoadsorption columns are listed in the eudamed database, which is the EU’s central registry for medical devices. This registration ensures transparency and compliance with EU regulatory requirements for Class IIb devices.

How are VitroSorb AB’s devices classified under medical device regulations?

VitroSorb AB’s immunoadsorption columns fall under Class IIb classification. This classification is determined based on the risk associated with the device’s intended use—here, modifying patient plasma to address blood type incompatibility in organ transplantation—which requires a higher level of scrutiny than lower-risk devices but is not considered high-risk like Class III.

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

Information

Country
Sweden
Address
41, Per Albin Hanssons Väg, MALMÖ, Sweden
Phone
0735138200
PRRC contact
Ulf Lundgren
EUDAMED SRN
SE-MF-000034941