•          The VARIANT™ nbs System is the established worldwide standard in automated newborn screening for sickle cell disease and other hemoglobin disorders:
  •          Detects presence of hemoglobins (F, A, S, D, C, E) that are clinically significant for identification of the presence of:

-          hemoglobin disorders

-          carrier status for abnormal hemoglobins

-          double heterozygote conditions

  •          Walk away automation
  •          High capacity – up to 1,128 samples per run
  •          Positive sample tracking with on-board barcode reader
  •          Confidence with FDA clearance for dried blood spot samples
  •          High resolution separation with Bio-Rad HPLC
  •          “Smart” reports with suggested patterns
  •          Easier results review with the pattern filter
  •      Streamlined workflow with results and chromatograms export to LIS