Cepheid Xpert HIV-1 Qual XC Сінгапур - англійська - HSA (Health Sciences Authority)

cepheid xpert hiv-1 qual xc

spd scientific pte ltd - immunology - xpert® hiv-1 qual xc (extended coverage) is an in vitro nucleic acid amplification test for the qualitative detection of human immunodeficiency virus type 1 (hiv-1) total nucleic acids, on the automated genexpert® system. the test is used to detect hiv-1 in human dried blood spots (dbs) and edta capillary or venous whole blood (wb) specimens from individuals suspected of hiv-1 infection. xpert® hiv-1 qual xc is intended to aid in the diagnosis of hiv-1 infection in conjunction with clinical presentation and other laboratory markers in infant, adolescent and adult populations. xpert® hiv-1 qual xc is intended to be used by laboratory professionals, trained health care professionals or other health care workers receiving appropriate training on the use of the device. this test may be used in laboratory or near-patient testing environments. the test is not intended to be used as a blood, organ or tissue donor screening test for hiv-1.

Diasorin LIAISON Measles IgG Сінгапур - англійська - HSA (Health Sciences Authority)

diasorin liaison measles igg

spd scientific pte ltd - immunology - the liaison® measles igg assay uses chemiluminescence immunoassay (clia) technology for the semi- quantitative determination of specific igg antibodies to measles virus in human serum samples. it is intended to be used as an aid in the determination of serological status to measles virus. the test has to be performed on the liaison® analyzer family.

Diasorin LIAISON Mumps IgG Сінгапур - англійська - HSA (Health Sciences Authority)

diasorin liaison mumps igg

spd scientific pte ltd - immunology - the liaison® mumps igg assay uses chemiluminescence immunoassay (clia) technology for the semi- quantitative determination of specific igg antibodies to mumps virus in human serum samples. it is intended to be used as an aid in the determination of serological status to mumps virus. the test has to be performed on the liaison® analyzer family.

DiaSorin LIAISON VZV IgG Сінгапур - англійська - HSA (Health Sciences Authority)

diasorin liaison vzv igg

spd scientific pte ltd - immunology - the liaison® vzv igg assay uses chemiluminescence immunoassay (clia) technology for the quantitative determination of specific igg antibodies to varicella-zoster virus (vzv) in human serum samples. the test has to be performed on the liaison® analyzer family

DiaSorin LIAISON Mycoplasma pneumoniae IgG Сінгапур - англійська - HSA (Health Sciences Authority)

diasorin liaison mycoplasma pneumoniae igg

spd scientific pte ltd - immunology - the liaison® mycoplasma pneumoniae igg assay uses chemiluminescence immunoassay (clia) technology for the semi-quantitative determination of specific igg antibodies to mycoplasma pneumoniae in human serum samples. the test has to be performed on the liaison® analyzer family.

Diasorin LIAISON Mycoplasma pneumoniae IgM Сінгапур - англійська - HSA (Health Sciences Authority)

diasorin liaison mycoplasma pneumoniae igm

spd scientific pte ltd - immunology - the liaison® mycoplasma pneumoniae igm assay uses chemiluminescence immunoassay (clia) technology for the qualitative determination of specific igm antibodies to mycoplasma pneumoniae in human serum samples. the test has to be performed on the liaison® analyzer family.

ELITechGroup VZV ELITe MGB kit Сінгапур - англійська - HSA (Health Sciences Authority)

elitechgroup vzv elite mgb kit

spd scientific pte ltd - microbiology - the «vzv elite mgb® kit» product is an in vitro diagnostic medical device intended to be used by healthcare professionals as a qualitative nucleic acids amplification assay for the detection of the dna of human herpetic varicella - zoster virus (vzv) in clinical samples. the assay was validated in association with elite ingenius® system starting form cerebrospinal fluid (csf), whole blood collected in edta, and plasma collected in edta. the product is intended for use as an aid in the diagnosis of vzv infections alongside clinical data of the patient and other laboratory tests outcomes.

Cepheid Xpert MTBXDR Сінгапур - англійська - HSA (Health Sciences Authority)

cepheid xpert mtbxdr

spd scientific pte ltd - microbiology - the xpert mtb/xdr test, performed on the genexpert instrument systems, is a qualitative, nested real-time polymerase chain reaction (pcr) in vitro diagnostic test for the detection of extensively drug resistant (xdr) mycobacterium tuberculosis (mtb) complex dna in unprocessed sputum samples, concentrated sediments prepared from sputum, or bd™ mycobacterial growth indicator tube (mgit™) culture. in specimens where mtb is detected, the xpert mtb/xdr test can also detect isoniazid (inh) resistance associated mutations in the katg and fabg1 genes, oxyr-ahpc intergenic region and inha promoter; ethionamide (eth) resistance associated with inha promoter mutations only; fluoroquinolone (flq) resistance associated mutations in the gyra and gyrb quinolone resistance determining regions (qrdr); and second line injectable drug (slid) associated mutations in the rrs gene and the eis promoter region.

Diasorin LIAISON Direct Renin Сінгапур - англійська - HSA (Health Sciences Authority)

diasorin liaison direct renin

spd scientific pte ltd - immunology - the liaison® direct renin assay uses chemiluminescence immunoassay (clia) technology for the in vitro quantitative determination of renin in human edta-plasma specimens. renin measurement is of help in the diagnosis and treatment of a number of hypertension types in humans. the test has to be performed on the liaison® analyzer family.

ELITechGroup CMV ELITe MGB Kit Сінгапур - англійська - HSA (Health Sciences Authority)

elitechgroup cmv elite mgb kit

spd scientific pte ltd - microbiology - the «cmv elite mgb® kit» product is an in vitro diagnostic medical device intended to be used by healthcare professionals as a qualitative nucleic acids real-time pcr assay for the detection of the dna of human cytomegalovirus (cmv) extracted from clinical specimens. the assay is validated in association with the «elite ingenius» instrument, automated and integrated system for extraction, real-time pcr and results interpretation, using human specimens of whole blood collected in edta (wb), plasma collected in edta (pl). the product is intended for use as an aid in the diagnosis of cmv infections. the results must be interpreted in combination with all relevant clinical observations and laboratory outcomes.