ASO Latex Test Kit:Diagnostic Automation Inc. Latex agglutination slide test for
ASO Latex Test Kit:Diagnostic Automation Inc. Latex agglutination slide test for the Qualitative and Semi-quantitative determination of Antistreptolysin-O in non-diluted serum.
AccuDiag™ Cytomegalovirus IgM ELISAA collection of reagents and other associated
AccuDiag™ Cytomegalovirus IgM ELISAA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to cytomegalovirus (CMV) in a clinical specimen, using an enzyme immunoassay (EIA) method.
AccuDiag™Measles IgM ELISA KitA collection of reagents and other associated mate
AccuDiag™Measles IgM ELISA KitA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to Measles virus in a clinical specimen, using an enzyme immunoassay (EIA) method.
AccuDiag™ sTfR - Soluble Transferrin Receptor ELISA KitA collection of reagents
AccuDiag™ sTfR - Soluble Transferrin Receptor ELISA KitA collection of reagents and other associated materials intended to be used for the quantitative measurement of soluble transferrin receptor protein in a clinical specimen, using an enzyme immunoassay (EIA) method.
AccuDiag™ RF Latex Test KitFor the qualitative and semi-quantitative measurement
AccuDiag™ RF Latex Test KitFor the qualitative and semi-quantitative measurement of RF in human serum.
AccuDiag™CRP Latex Test KitC- Reactive Protein (CRP) latex slide test is used fo
AccuDiag™CRP Latex Test KitC- Reactive Protein (CRP) latex slide test is used for the qualitative and semi-quantitative measurement of C-reactive protein (CRP) in human serum.
OneStep hCG Combo Urine/Serum RapiCard™ InstaTestA collection of reagents and ot
OneStep hCG Combo Urine/Serum RapiCard™ InstaTestA collection of reagents and other associated materials intended to be used for the qualitative and/or semi-quantitative detection of total human chorionic gonadotropin (HCG), which may include intact HCG, nicked HCG, free alpha-HCG subunits and/or free beta-HCG subunits, in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method.
Diagnostic Automation Inc. URS-2P (100 Strips Bottle) for the semi-quantitative
Diagnostic Automation Inc. URS-2P (100 Strips Bottle) for the semi-quantitative and qualitative detection of Glucose and Protein in Urine.
JIL,JIR
Method, Enzymatic, Glucose (Urinary, Non-Quantitative),Indicator Method, Protein
Method, Enzymatic, Glucose (Urinary, Non-Quantitative),Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)
The DA50TS8 Microplate Washer is a compact microplate washing system with functi
The DA50TS8 Microplate Washer is a compact microplate washing system with functionality that is unsurpassed in its class. The 4.3” color LCD touchscreen provides a visual interface with menu-driven programming that makes creating protocols fast and intuitive. The DAW50TS is an affordable choice for automating the wash steps of a variety of applications in clinical and research laboratories. Used in conjunction with the DAR800TS Absorbance Reader or other detection systems, the DAW50TS offers a welcome upgrade from manual processing - bringing convenience and consistently high-quality results to your laboratory’s plate washing workflows.
DA800TS Microplate Reader is an affordable, high-quality microplate reader for a
DA800TS Microplate Reader is an affordable, high-quality microplate reader for assays in 6- to 96-well formats. The color touchscreen provides a visual user interface, making programming simple. The onboard software includes “quick read” and custom protocols, with data viewed immediately after measure, followed by export to USB or to the compact printer.
JJQ
Colorimeter, Photometer, Spectrophotometer For Clinical Use
AccuDiag ™ Gliadin IgGMultiple Coeliac disease-associated antibody IVD, kit, enz
AccuDiag ™ Gliadin IgGMultiple Coeliac disease-associated antibody IVD, kit, enzyme immunoassay (EIA)AccuDiag ™ Gliadin IgG ELISA Gliadin IgG Test System is intended for the qualitative and semi-quantitative detection of IgG-class antibodies to gliadin in human serum. The Test System is intended to be used as an aid in the diagnosis of gastrointestinal disorders, mainly Celiac Disease. This test is for In Vitro diagnostic use.
AccuDiag ™ Rheumatoid factor IVD, kit, enzyme immunoassay (EIA)The Diagnostic A
AccuDiag ™ Rheumatoid factor IVD, kit, enzyme immunoassay (EIA)The Diagnostic Automation Rheumatoid Factor (RF) Enzyme-Linked Immu-nosorbent Assay (ELISA) is intended for the detection of IgM antibodies in human serum to RF antigen and as an aid in the diagnosis of rheumatoid arthritis. For in vitro diagnostic use. High complexity test.
AccuDiag ™ SSB/La antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EI
AccuDiag ™ SSB/La antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EIA). A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of anti-SSB or anti-La antibodies (Sjogren's antibodies) in a clinical specimen, using an enzyme immunoassay (EIA) method.
AccuDiag ™ SSA/Ro antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EI
AccuDiag ™ SSA/Ro antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EIA)The SS-A Test System is a semi-quantitative immunoassay for the detection of IgG antibodies to SSA in human sera. When performed according to these instructions, the results of this assay may aid in the diagnosis and treatment of autoimmune connective tissue disorders. A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of anti-SSA or anti-Ro antibodies (Sjogren's antibodies) in a clinical specimen, using an enzyme immunoassay (EIA) method.
AccuDiag ™ IFA FTA-ABS Test System - Treponema pallidum total antibody IVD, kit,
AccuDiag ™ IFA FTA-ABS Test System - Treponema pallidum total antibody IVD, kit, Fluorescent ImmunoassayFluorescent Treponemal Antibody-Absorption (FTA-ABS) Test System is designed for the qualitative determination of antibodies to Treponema pallidum, and is intended to be used as an aid in the confirmation of syphilis antibodies. A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of total antibodies to Treponema pallidum in a clinical specimen using a fluorescent immunoassay method. The assay is designed to detect infection with Treponema pallidum, the bacteria associated with syphilis.
AccuDiag ™ ANCA Screen IgG ELISA Kit A collection of reagents and other associa
AccuDiag ™ ANCA Screen IgG ELISA Kit A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative screening for one or multiple antibodies associated with vasculitis in a clinical specimen, using an enzyme immunoassay (EIA) method. The assayed antibodies may include autoimmune antibodies directed at the glomerular basement membrane (GBM), anti-neutrophil cytoplasmic antibodies to myeloperoxidase (ANCA MPO) and/or anti-neutrophil cytoplasmic antibodies to proteinase-3 (PR3).
MOB
Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
AccuDiag ™ Strongyloides IgG ELISAThe Strongyloides ELISA test is a qualitative
AccuDiag ™ Strongyloides IgG ELISAThe Strongyloides ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to Strongyloides, in samples of human serum or plasma.
AccuDiag ™ Toxocara IgG ELISAThe Toxocara ELISA test is a qualitative enzyme imm
AccuDiag ™ Toxocara IgG ELISAThe Toxocara ELISA test is a qualitative enzyme immunoassay for the detection of antibodies to Toxocara, in samples of human serum or plasma.
AccuDiag ™ RPR Latex Test KitA collection of reagents and other associated mater
AccuDiag ™ RPR Latex Test KitA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of non-specific reagin antibodies that are produced in response to infection with Treponema pallidum bacteria, in a clinical specimen using an agglutination method [for example Rapid Plasma Reagin (RPR) test or Venereal Disease Research Laboratory (VDRL) test]. The assay is designed to detect infection with Treponema pallidum, the bacteria associated with syphilis.
AccuDiag ™ Mumps IgMA collection of reagents and other associated materials inte
AccuDiag ™ Mumps IgMA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to Mumps virus in a clinical specimen, using an enzyme immunoassay (EIA) method.
AccuDiag ™ Cytomegalovirus (CMV) IgG is an enzyme-linked immunosorbent assay (E
AccuDiag ™ Cytomegalovirus (CMV) IgG is an enzyme-linked immunosorbent assay (ELISA) for the qualitative detection of IgG class antibodies to cytomegalovirus in human serum. This test is intended to be used to evaluate serologic evidence of previous or primary infection with CMV.
AccuDiag ™ Herpes Simplex Virus (HSV) 1 & 2 IgM ELISA is an enzyme-linked immuno
AccuDiag ™ Herpes Simplex Virus (HSV) 1 & 2 IgM ELISA is an enzyme-linked immunosorbent assay for the qualitative detection of IgM class antibodies to Herpes Simplex Virus (HSV) in human serum. This test is intended to be used to evaluate serologic evidence of primary or reactivated infection with HSV and is for In Vitro diagnostic use.
AccuDiag ™ Rubella IgG ELISA is designed for the qualitative and/or quantitative
AccuDiag ™ Rubella IgG ELISA is designed for the qualitative and/or quantitative detection of IgG antibodies to rubella virus in human serum. This test is intended to be used to evaluate single sera for immune status or paired sera to demonstrate seroconversion, and is for In Vitro diagnostic use.
OPL
Multiplex Immunoassay For Measles Virus, Mumps Virus, Rubella And Varicella Zoster Virus
AccuDiag ™ Borrelia burgdorferi IgG/IgM is an enzyme-linked immunosorbent assay
AccuDiag ™ Borrelia burgdorferi IgG/IgM is an enzyme-linked immunosorbent assay (ELISA) for the qualitative presumptive detection of total (IgG and IgM) antibodies to Borrelia burgdorferi in human serum. This ELISA should only be used for patients with signs and symptoms that are consistent with Lyme disease. Equivocal or positive results must be supplemented by testing with a standardized Western blot procedure. Positive supplemental results are supportive evidence of exposure to B. burgdorferi and can be used to support a clinical diagnosis of Lyme disease.
The cTnI ELISA is intended for the quantitative determination of cardiac troponi
The cTnI ELISA is intended for the quantitative determination of cardiac troponin I in human serum. Measurement of troponin I values are useful in the evaluation of acute myocardial infarction (AMI).
TROPONIN I (HUMAN CARDIAC-SPECIFIC) ENZYME IMMUNOASSAY TEST KIT
Lateral Flow immunoassay for the qualitative determination of Myoglobin, Troponi
Lateral Flow immunoassay for the qualitative determination of Myoglobin, Troponin I, and CK-MB in Human Heparinized Whole Blood, Plasma, or Serum.
Cardiac STATus Myoglobin/Troponin I/CK-MB Tandem Test
Lateral Flow immunoassay for the qualitative determination of Troponin I in Huma
Lateral Flow immunoassay for the qualitative determination of Troponin I in Human Heparinized Whole Blood, Plasma, or Serum.
Lateral Flow immunoassay for the qualitative determination of Myoglobin, Troponi
Lateral Flow immunoassay for the qualitative determination of Myoglobin, Troponin I, and CK-MB in Human Heparinized Whole Blood, Plasma, or Serum.
Cardiac STATus Myoglobin/Troponin I/CK-MB Tandem Test
Lateral Flow immunoassay for the qualitative determination of Troponin I in Huma
Lateral Flow immunoassay for the qualitative determination of Troponin I in Human Heparinized Whole Blood, Plasma, or Serum.
Lateral Flow immunoassay for the qualitative determination of Myoglobin, Troponi
Lateral Flow immunoassay for the qualitative determination of Myoglobin, Troponin I, and CK-MB in Human Heparinized Whole Blood, Plasma, or Serum.
Cardiac STATus Myoglobin/Troponin I/CK-MB Tandem Test
Lateral Flow immunoassay for the qualitative determination of Troponin I in Huma
Lateral Flow immunoassay for the qualitative determination of Troponin I in Human Heparinized Whole Blood, Plasma, or Serum.
Access hsTnI is a paramagnetic particle, chemiluminescent immunoassay for the qu
Access hsTnI is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of cardiac troponin I (cTnI) levels in human serum and plasma using the UniCel DxI Access Immunoassay Systems to aid in the diagnosis of myocardial infarction (MI).Access hsTnI is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of cardiactroponin I (cTnI) levels in human serum and plasma using the Access 2 Immunoassay Systems to aid in the diagnosisof myocardial infarction (MI).
The Access AccuTnI+3 Reagent is a paramagnetic particle, chemiluminescent immuno
The Access AccuTnI+3 Reagent is a paramagnetic particle, chemiluminescent immunoassay for the highly sensitive quantitative determination of cardiac troponin I (cTnI) levels in human serum and plasma using the UniCel DxI Immunoassay System to aid in the diagnosis of myocardial infarction.
The Access AccuTnI+3 Reagent is a paramagnetic particle, chemiluminescent immuno
The Access AccuTnI+3 Reagent is a paramagnetic particle, chemiluminescent immunoassay for the highly sensitive quantitative determination of cardiac troponin I (cTnI) levels in human serum and plasma using the Access 2 Immunoassay System to aid in the diagnosis of myocardial infarction.
The cTnI ELISA is intended for the quantitative determination of cardiac troponi
The cTnI ELISA is intended for the quantitative determination of cardiac troponin I in human serum. Measurement of troponin I values are useful in the evaluation of acute myocardial infarction (AMI).
TROPONIN I (HUMAN CARDIAC-SPECIFIC) ENZYME IMMUNOASSAY TEST KIT
VIDAS ® Troponin I Ultra (TNIU) is an automated quantitative test for use on the
VIDAS ® Troponin I Ultra (TNIU) is an automated quantitative test for use on the VIDAS instruments for the determination of human cardiac troponin I in human serum or plasma.