Profile: Absorber AB develops products for allogeneic transplantation. Our Xm-One® test can detect antibody population, which is not possible to detect with lymphocyte crossmatch tests that are strongly associated with rejection episodes and reduced kidney function after transplantation. It can identify patients who are at risk of antibody-mediated rejections.
FDA Registration Number: 3005287147
US Agent: Anders Hellstrom /
Phone: +1-(847)-446-7683 Fax: +1-()- - E-Mail:
3 Products/Services (Click for related suppliers)
|• Immunodiagnostic Test Kits|
|• Non-Diagnostic Qualitative Test For Hla (FDA Code: MZI)|
|• Positive and Negative Febrile Antigen Control Serum (FDA Code: GSN / 866.3085)|