We offer detection systems with differentiated specificities and sensitivities that enable efficient and reliable microscopic detection of antigenic structures in cells and tissue sections, depending on the application and method used. Our detection systems are constantly being developed and improved.
We have declared the conformity of its CE/IVD-labeled products of risk class A (e.g. detection reagents) according to IVDR in time for the start of application of Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) on 26.05.2022. Thus, these risk class A products fulfill all requirements of the IVDR.
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