DBS Sample Collection Kit - Neonatal Screening

Comprehensive newborn screening solution combining diagnostic kits, instruments, and software for early detection of rare congenital and metabolic diseases. Enables laboratories to identify genetic predispositions and support pharmacogenetic testing without DNA extraction requirements, streamlining workflow from sample collection to clinical results.

Comprehensive newborn screening solution for detecting inborn errors of metabolism and genetic disorders in neonates within the first days of life. Uses fluorometric microplate-based assays for high-sensitivity detection of metabolic conditions such as phenylketonuria.

Molecular diagnostic kit for screening blood samples for infectious pathogens including viruses and bacteria. Supports blood safety testing in transfusion and donation screening programs.

Tandem mass spectrometry and immunoassay reagents for congenital disease screening. Critical for early detection of metabolic and endocrine disorders.

Newborn screening test for early detection of metabolic, hemoglobin, and functional disorders in newborns. Enables timely clinical intervention to prevent serious health complications and developmental delays. Supports public health programs and hospital-based screening protocols.

Diagnostic test kit designed for assessment of maternal and neonatal health biomarkers during pregnancy and postpartum periods. Supports prenatal and pediatric health monitoring.

Comprehensive screening platform for early detection of genetic and metabolic disorders in newborns. Delivers rapid, accurate results to support timely clinical intervention and improved patient outcomes.

An FDA-registered Class II medical device dried blood spot collection card specifically designed for neonatal screening and testing applications in the EU. The card enables safe collection and transportation of blood samples from newborns for diagnostic analysis.

Testing system for perinatal disease screening and risk assessment in pregnant women and newborns. Supports maternal-fetal health monitoring protocols.

Newborn screening system for automated detection of metabolic and genetic disorders. Available in standard and enhanced versions for screening of bloodspot samples.

Next-generation sequencing-based detection kit screening over 165 preventable genetic and metabolic diseases in newborns. Uses proprietary All-in-One PCR amplicon capture technology combined with NGS for early diagnosis and intervention.

Molecular diagnostic kit for screening pregnant women and newborns for infectious diseases and genetic conditions. Supports prenatal and perinatal health monitoring programs.