Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - obstetrics & gynaecology - bio-rad bioplex 2200 torc igm kit is a multiplex flow immunoassay intended for the qualitative detection of igm antibodies to toxoplasma gondii (t.gondii), rubella and cytomegalovirus (cmv) in human serum and edta or heparinized plasma. this kit is intended as an aid in the diagnosis or presumptive diagnosis of an acute or recent t.gondii, rubella and/or cmv infection in pregnant women and individual suspected of having one or more of the respective disease states.

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - clinical chemistry - bio-rad d10 dual consists of the short program and the extended program. bio-rad d10 dual short program is intended for the percent determination of hemoglobin a1c in human whole blood using ion-exchange high performance liquid chromatography (hplc). bio-rad d-10 extended program is intended for the percent determination of hemoglobins a2, f, and a1c, and for the detection of abnormal hemoglobins in human whole blood using ion-exchange high-performance liquid chromatography (hplc).

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - microbiology - the fast test device uses the immunochromatography (ict or lateral migration) technique to detect anti-hiv-1 and anti-hiv-2 antibodies in human serum, plasma, venous blood and capillary blood. this kit is not intended for blood donor screening. any sample found to be reproducibly positive must be confirmed using an appropriate method (western-blot or equivalent) to prove the presence of anti-hiv antibodies.

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad genscreen® hiv 1/2 version 2 is an immunoassay based on the principle of a two-step sandwich technique for the detection of the various antibodies associated with hiv1 and/or hiv2 virus in human serum or plasma.

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad kallestad crithidia luciliae kit is intended as an indirect fluorescent antibody (ifa) procedure for the detection and semi-quantitation of human native ndna auto-antibodies.the detection and semi-quantitation of autoantibodies aid in the diagnosis of autoimmune diseases.

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad kallestad hep-2 kit is intended for the detection and semi-quantitation of human nuclear autoantibodies using indirect fluorescent antibody procedure.

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad bioplex 2200 torc igg kit is a multiplex flow immunoassay intended for the quantitative detection of igg antibodies to toxoplasma gondii (t.gondii) and rubella and the qualitative detection of igg antibodies to cytomegalovirus (cmv) in human serum and edta or heparinized plasma. this kit is intended as an aid in the determination of serological status to t.gondii, rubella and cmv. this kit is not intended for use in screening blood or plasma donors.

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad liquichek ana control, centromere pattern, positive is intended for use as an unassayed quality control to monitor indirect immunofluorescent testing of antinuclear antibodies (ana).

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad liquichek ana control, homogeneous pattern, positive is intended for use as an unassayed quality control to monitor indirect immunofluorescent testing of antinuclear antibodies (ana).

Singapore - English - HSA (Health Sciences Authority)

bio-rad laboratories (singapore) pte ltd - immunology - bio-rad liquichek ana control, mitotic spindle pattern is intended for use as an unassayed quality control to monitor indirect immunofluorescent testing of antinuclear antibodies (ana).