Labsystems Diagnostics is based in Finland and has been a forerunner in innovative diagnostic research and development for nearly 40 years, pioneering new technologies for newborn screening and point of care testing. Among the market leaders in newborn screening, our neonatal products save and improve the lives of babies in more than 70 countries. Being a one-stop solution provider for newborn screening, offering the most comprehensive and high quality screening kits, supported by best-in-class automation capabilities and user friendly software, we have a strong record of technology leadership, including pioneering research to enable the early detection of diseases.

Labsystems Diagnostics was the first to:

  • Develop fluorometric PKU [Phenylketonuria] tests for NBS
  • Provide PKU assays in micro-plate format

We continue to invest in our R&D and are strongly committed to developing innovative newborn diagnostics solutions at our state of the art production facility in Vantaa, Finland.

Besides newborn screening, our core competencies and capabilities include point of care testing, molecular testing, immunoassay development, automated manufacturing and mass spectrometry solutions. With a thriving commercial organization around the world, Labsystems Diagnostics remains steadfast in serving its customers through high quality products and solutions that met the required regulatory and safety standards.

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Labsystems Diagnostics’ Neonatal Biotinidase kit is for enzymatic determination of biotinidase enzyme activity from blood samples dried on filter paper, with fluorometric detection, intended for newborn screening for biotinidase deficiency.

Labsystems Diagnostics’ Neonatal G6PD is an enzymatic method for the quantitative determination of glucose-6-phosphate dehydrogenase activity in blood samples dried on filter paper, with fluorometric detection, intended for newborn screening of glucose-6-phosphate dehydrogenase deficiency.

Labsystems Diagnostics’ Neonatal Galactose is a quantitative fluorometric test for the total galactose from dried blood spot samples. The test is based on the combined determination of free and galactose liberated from the cleavage of the galactose-1-phosphate.

Labsystems Diagnostics’ test is designed for the quantitative in vitro determination of galactose-1-phosphate uridyltransferase (GALT) activity in blood samples dried on filter paper. This kit is intended for screening newborns for classic galactosemia, which is caused by the inability to convert Galactose-1-phosphate into glucose-

Labsystems Diagnostics’ Neonatal Phenylalanine is a chemical method, with fluorometric detection, for quantitative determination of phenylalanine from blood specimens dried on filter paper, intended for newborn screening for phenylketonuria (PKU).

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Labsystems Diagnostics’ Neonatal 17-OH-Progesterone FEIA test is a fluorometric enzyme immunoassay enabling the quantification of 17-hydroxyprogestrone steroid present in blood samples dried on filter paper. The test can be used for the screening of newborn for Congenital Adrenal Hyperplasia (CAH).

Labsystems Diagnostics’ Neonatal hTSH FEIA Plus is a  fluorometric enzyme immunoassay for the quantitative determination of human thyroid stimulating hormone (hTSH, human thyrotropin) in blood samples dried on filter paper as a primary test for screening of babies for congenital hypothyroidism (CH).

Labsystems Diagnostics’ Neonatal IRT FEIA is a fluorometric enzyme immunoassay for the quantitative determination of human immuno reactive trypsinogen (IRT) from blood samples dried on filter paper as a primary test for screening of babies for cystic fibrosis (CF).

Fluorometric enzyme immunoassay for the quantitative determination of total Thyroxine (T 4) from blood samples dried on filter paper as a primary test for screening of babies for congenital hypothy­roidism (CH).

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Labsystems Diagnostics’ SCID-SMA Real-Time PCR kit is intended for rapid and simultaneous detection of severe combined immunodeficie SCIO) syndrome and Spinal muscular atrophy (SMA) in newborns by using DNA samples either from whole blood or dried blood spots, after DNA extraction

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Instrument

To run a successful and cost-effective newborn screening test, there is a requirement for all the instruments and reagents. Trivitron’s Labsystems Diagnostics Oy delivers the most sophisticated fully-automated solutions in the highest quality and performance standards, ensuring the highest levels of performance for your lab.

Newborn Screening Automate NS2400

REVOLUTIONARY NS2400 NEONATAL SCREENING AUTOMATE With 25 plate capacity, 10 Assays on board, NS2400 automates the highest throughput sites or can handle the highest workload with extremely flexible, could be customized to your needs

Automatic NS496 Plus

NS496 plus DBS puncher with air humidification system and clean punch mechanism designed to automate laboratory automate system and is used to punch dried blood spot samples into a 96 wellmicrotitre plates for subsequent analysis

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Labsystems Diagnostics introduced world’s first fluorometric microplate based assay for screening Phenyl Alanine in newborns to detect Phenylketonuria (PKU) and now on tandem MS along with more than 50 disorders. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) increased the screening possibilities by monitoring levels of amino acids and acylacarnitines. These tests can also be used in screening positive samples as a second tier confirmation test to differentiate between true and false positive samples. LC-MS/MS can detect several disorders with a single injection, which is important in high throughput labs

Neomass AAAC Plus

Expanded newborn screening panel for quantitative determination of 15 Amino acids, free Carnitines, 12 Acylcarnitines, Argininosuccinic acid (ASA) and Succinylacetone (SUAC) under the same extraction method and single injection/single run step without using any toxic compounds, on Tandem MS

Quantitative Analysis of:

  • 15 Amino Acids
  • 13 Acyl Carnitines
  • Argininosuccinic Acid (ASA)
  • Succinylacetone (SUAC)

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