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Lacar MDX Technologies

Belgium BE-MF-000001212 Last updated 25 Oct 2026

Devices
129
Registries
EUDAMEDFDA
FDA recalls
0

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About

Enhance your lab's performance with high-quality diagnostic solutions. We specialize in newborn screening, pharmacogenetics, and genetic predispositions & disorders. From samples to results, we provide high-quality kits, instruments & software.

From the manufacturer's own website. Source

What Lacar MDX Technologies makes

LaCAR MDx Technologies manufactures in vitro diagnostic kits for newborn screening, including assays for hemoglobins, thyroid-stimulating hormone (TSH), total thyroxine (T4), biotinidase, immunoreactive trypsinogen (IRT), and maple syrup urine disease (MSUD) using methods such as ELISA, fluorescence, and tandem mass spectrometry (MS/MS). The company also produces LAMP-based kits for detecting HLA variants associated with celiac disease and PAI-1 mutations.

The manufacturer's devices are classified as Class A IVD General and are listed in the EUDAMED database. LaCAR MDx Technologies is based in Belgium (BE).

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does LaCAR MDx Technologies make?

LaCAR MDx Technologies manufactures in vitro diagnostic kits for newborn screening, including assays for hemoglobins, thyroid-stimulating hormone (TSH), total thyroxine (T4), biotinidase, immunoreactive trypsinogen (IRT), and maple syrup urine disease (MSUD) using methods such as ELISA, fluorescence, and tandem mass spectrometry (MS/MS). The company also produces LAMP-based kits for detecting HLA variants associated with celiac disease and PAI-1 mutations.

Where is LaCAR MDx Technologies based?

LaCAR MDx Technologies is based in Belgium, as indicated by the country code BE in the provided data.

Which regulatory registry lists LaCAR MDx Technologies' devices?

LaCAR MDx Technologies' devices are listed in the EUDAMED database, which is the European database on medical devices and in vitro diagnostic medical devices.

How are LaCAR MDx Technologies' devices classified?

LaCAR MDx Technologies' devices are classified as Class A IVD General, indicating they are in vitro diagnostic devices with low risk according to the European regulatory framework.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Belgium(from SRN)
Address
10, Rue des Chasseurs Ardennais, Liège, Belgium
Phone
+32 4 287 39 44
PRRC contact
Cédric Remy
EUDAMED SRN
BE-MF-000001212
FDA FEI number
3042250641
DUNS number
371365041