Comprehensive screening tests for detection of inborn errors of metabolism in neonates, identifying genetic and metabolic disorders within the first days of life to enable early intervention.
Manufactured by
Trivitron Healthcare Private Limited
Chennai, India
Right from the fetus stage, quality healthcare becomes our fourth basic need. When the wheels started to roll, technology evolved, and now it is transforming healthcare, making it better and affordable. Several innovations saved time, empowered many to eliminate the expensive price tag, and made the cure possible. Since 1997, the journey of Trivitron Healthcare as a medical technology company providing affordable healthcare solutions has woven a fascinating thread of inspiration for many healthcare providers. Trivitron markets its products to hospitals, individual healthcare providers, independent clinics and laboratories, extended care facilities, renal care centers, and all other roofs providing healthcare solutions. As a pioneer in the field, Trivitron constantly pursues technological innovations to offer superior clinical benefits at a lower cost. At Trivitron, quality healthcare is considered a fundamental right, and the vision is to make it available for people of all classes across geographies and economic backgrounds.
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3 of 65 closest product alternatives
Fortress Diagnostics Limited · United Kingdom
In vitro diagnostic tests for screening of metabolic and genetic disorders in newborns. Used to detect treatable conditions early for improved patient outcomes.
Shandong Kanghua Biotechnology Co.,Ltd. · China
Diagnostic tests for prenatal screening and maternal health assessment including genetic and biochemical markers. Utilized for comprehensive obstetric care and fetal anomaly detection.
GUANGZHOU FENGHUA BIOENGINEERING CO.,LTD · China
Newborn screening assays for the detection of metabolic, endocrine, and functional disorders in newborns. These in vitro diagnostic tests enable early identification of conditions such as congenital hypothyroidism, phenylketonuria, and other inherited metabolic diseases through blood spot analysis. Results support timely clinical intervention and prevention of severe developmental complications.
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