This information is intended for physicians and healthcare professionals only.
ID CORE XT, ID HPA XT, ID RHD XT, BIDS XT, and ID CORE CONTROL comply with the Directive 98/79/EC of the European Parliament and of the Council on in vitro diagnostic medical devices. CE mark certification.
ID CORE XT, ID CORE CONTROL, and BIDS XT are sold in the US as IVD (FDA).
ID HPA XT and ID RHD XT are sold in the US for research use only (RUO). Not for use in diagnostic procedures.
Product registration and availability vary by country. Ask your local Grifols representative for more information or contact us here.