Directive 98/79/EC of the European Parliament and of the CouncilDangos y teitl llawn

Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices

  • Reagents and reagent products, including related calibrators and control materials, for determining the following blood groups: anti-Duffy and anti-Kidd,

  • reagents and reagent products, including related calibrators and control materials, for determining irregular anti-erythrocytic antibodies,

  • reagents and reagent products, including related calibrators and control materials, for the detection and quantification in human samples of the following congenital infections: rubella, toxoplasmosis,

  • reagents and reagent products, including related calibrators and control materials, for diagnosing the following hereditary disease: phenylketonuria,

  • reagents and reagent products, including related calibrators and control materials, for determining the following human infections: cytomegalovirus, chlamydia,

  • reagents and reagent products, including related calibrators and control materials, for determining the following HLA tissue groups: DR, A, B,

  • reagents and reagent products, including related calibrators and control materials, for determining the following tumoral marker: PSA,

  • reagents and reagent products, including related calibrators, control materials and software, designed specifically for evaluating the risk of trisomy 21,

  • the following device for self-diagnosis, including its related calibrators and control materials: device for the measurement of blood sugar.