Press releases and announcements

Gent, Belgium: July 16, 2017 – Fujirebio Europe today announced the CE-marking of the Lumipulse G Total Tau assay for its fully automated LUMIPULSE immunoassay systems. This CLEIA (chemiluminescent enzyme immunoassay) kit allows for the quantitative determination of total Tau in human cerebrospinal fluid within just 35 minutes.

Fujirebio Europe today announced the release of Lumipulse G HTLV-I/II, a CE-marked CLEIA (chemiluminescent enzyme immunoassay) test kit for in vitro diagnostic use with LUMIPULSE G system for qualitative detection of antibody to HTLV-I and HTLV-II in human serum or plasma for screening of HTLV-I/II viral infection.

Fujirebio Europe has announced the release of the Lumipulse G hs Troponin I assay for use in the diagnosis of Acute Myocardial Infarction (AMI). In addition, the company also launches its Lumipulse G Myoglobin assay, both assays providing precise and sensitive results in 35 minutes.

Fujirebio Europe today announced the release of the Lumipulse G β-Amyloid 1-42 assay for its fully automated LUMIPULSE immunoassay systems. This CE-marked CLEIA (chemiluminescent enzyme immunoassay) kit allows the quantitative measurement of β-amyloid1-42 in human cerebrospinal fluid within just 30 minutes. The Lumipulse G β-Amyloid 1-42 assay is based upon Fujirebio’s well established, pioneering ELISA-based INNOTEST® assay (the first neurodegeneration testing kit launched in 1995) and the know-how of Fujirebio in robust and automated CLEIA testing since the first LUMIPULSE instrument was released in 1992.

Since January 2nd 2017 Fujirebio Diagnostics AB (headquarters in Sweden) and Fujirebio Europe NV (headquarters in Belgium) share the same website, www.fujirebio-europe.com.

Fujirebio Europe today announced the release of Lumipulse G HMW Adiponectin, a biomarker useful in the diagnosis of insulin resistance in obesity and of metabolic syndrome, available on the fully automated LUMIPULSE G series of instruments.

Fujirebio Europe today announced the release of Lumipulse G whole PTH, a 3rd generation assay that is highly useful in the diagnostic of primary hyperparathyroidism, hypoparathyroidism as well as secondary hyperparathyroidism, mainly in nephrology. The Lumipulse G whole PTH is calibrated against the international standard NIBSC WHO 95/646.

Gent, Belgium: July 5th 2016 - Fujirebio Europe has launched a communication campaign under the title "A few drops of insight can lead to an ocean of understanding" intended to help doctors, nurses and healthcare workers explain to patients and their families the advantages of an early diagnosis of Alzheimer's Disease through CSF (Cerebrospinal fluid) testing.

Fujirebio Europe today announced the release of Lumipulse G BNP, its brain-type natriuretic peptide (BNP) assay for the fully automated LUMIPULSE G series. The assay allows for quantitative measurement of human BNP in human EDTA plasma in an in vitro diagnostics setting.

Fujirebio Europe today announced the release of the Lumipulse G Mesothelin assay for its fully automated LUMIPULSE G1200 immunoassay system. This CE-marked CLEIA (chemiluminescent enzyme immunoassay) kit allows for quantitative determination of Soluble Mesothelin Related Peptides (SMRP) in human serum or plasma within just 30 minutes.

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More than 50 years of pioneering expertise in IVD

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We are a global leader in the field of high quality in vitro diagnostics (IVD) testing. We have more than 50 years’ accumulated experience in the conception, development, production and worldwide commercialization of robust IVD products. Our IVD product lines span the range from specialized manual and automated testing to fully automated routine clinical laboratory testing solutions.

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