VitroSorb AB
Sweden SE-MF-000034941 Last updated 21 Oct 2026
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- Devices
- 3
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
SECORIM® ABO B-column Ref B-100
SECORIM® ABO A-column Ref A-100
SECORIM® ABO AB-Column Ref AB-100
About
Vitrosorb develops, produces and markets immunoadsorption columns aimed to eliminate the blood group barrier in organ transplantation.
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.
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.
Information
- Country
- Sweden
- Address
- 41, Per Albin Hanssons Väg, MALMÖ, Sweden
- Website
- www.vitrosorb.com
- [email protected]
- Phone
- 0735138200
- PRRC contact
- Ulf Lundgren
- EUDAMED SRN
- SE-MF-000034941