The Access hLH assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of luteinizing hormone (LH) levels in human serum and plasma using the Access Immunoassay Systems.

Access hLH Calibrators (33515) Intended Use: The Access hLH Calibrators are intended to calibrate the Access hLH assay for the quantitative determination of luteinizing hormone (LH) levels in human serum and plasma using the Access Immunoassay Systems.

The Access hFSH assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of follicle stimulating hormone (FSH) levels in human serum and plasma using the Access Immunoassay Systems.

The Access Total T3 assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of triiodothyronine levels in human serum and plasma using the Access Immunoassay Systems.

The Access Free T3 assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of free triiodothyronine levels in human serum and plasma using the Access Immunoassay Systems.

PK7400 Automated Microplate System

The Access Sensitive Estradiol assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of estradiol levels in human serum and plasma using the Access Immunoassay Systems.

DxC 700 AU Chemistry Analyzer

DxC 700 AU Chemistry Analyzer (with ISE)

DxC 700 AU Chemistry Analyzer, Direct Track Sampling

DxC 700 AU, Direct Track Sampling (with ISE)

AU480 Chemistry Analyzer

AU480 Chemistry Analyzer (with ISE)

AU680 Chemistry Analyzer

AU680 Chemistry Analyzer for Direct Track Sampling (with ISE)

AU680 Chemistry Analyzer (with ISE)

AU5800 Chemistry Analyzer

AU5800 Chemistry Analyzer, Automation-ready

The Access Ferritin assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of ferritin levels in human serum and plasma (heparin) using the Access Immunoassay Systems. Ferritin is used as an aid in the diagnosis of iron deficiency or iron overload.

The Access C-Peptide Calibrators are intended to calibrate the Access C-Peptide assay for the quantitative determination of C-peptide levels in human serum, plasma and urine using the Access Immunoassay Systems.

The Access C-Peptide assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of C-Peptide levels in human serum, plasma and urine using the Access Immunoassay Systems as an aid in the diagnosis and treatment of patients suspected of having diabetes or other insulin secretion disorders.

The Access HIV Ag/Ab combo assay is a paramagnetic particle, chemiluminescent immunoassay for the simultaneous qualitative in vitro detection and differentiation of HIV-1 p24 antigen and antibodies to HIV-1 (groups M and O) and/or HIV-2 in human pediatric (ages 2 through 21 years) and adult serum and serum separator tubes or plasma[lithium heparin, lithium heparin separator tubes, dipotassium (K2) EDTA, tripotassium (K3) EDTA, sodium citrate, acid-citrate-dextrose (ACD) and citrate phosphate-dextrose (CPD)] using the DxI 9000 Access Immunoassay Analyzer.The Access HIV Ag/Ab combo assay is intended to be used as an aid in the diagnosis of HIV-1 and/or HIV-2 infection, including acute or primary HIV-1 infection. The assay may also be used as an aid in the diagnosis of HIV-1 and/or HIV-2infection in pregnant women. The Access HIV Ag/Ab combo assay is for use on the DxI 9000 Access Immunoassay Analyzer only.This assay is not intended for use for screening donors of blood or blood products or human cells, tissues, or cellular or tissue-based products (HCT/Ps)

The Access HIV Ag/Ab combo Calibrators are intended to calibrate the Access HIV Ag/Ab combo assay for the simultaneous qualitative detection and differentiation of HIV-1 p24 antigen and antibodies to HIV-1 (groups M and O) and/or HIV-2 in human serum and plasma, using the DxI 9000 Access Immunoassay Analyzer.

The Access HIV Ag/Ab combo QC is intended for monitoring system performance of the Access HIV Ag/Ab combo assay. The Access HIV Ag/Ab combo QC is for use on the DxI 9000 Access Immunoassay Analyzer.

The Access PCT assay is a paramagnetic, chemiluminescent immunoassay for in vitro quantitative determination of procalcitonin (PCT) levels in human serum and plasma (lithium heparin and EDTA) using the Access Immunoassay Systems. Measurement of PCT in conjunction with other laboratory findings and clinical assessments aids in the risk assessment of critically ill patients on their first day of Intensive Care Unit (ICU) admission for progression to severe sepsis and septic shock.

DxC 500 AU Clinical Chemistry Analyzer

DxC 500 AU Clinical Chemistry Analyzer with ISE

DxH Concentrated ECO Diluent, when diluted to a working concentration, is an osmotically balanced, pH neutral solution of organic buffers, germicides, and sodium/potassium salts. The diluent acts as an electrolyte and cell volume stabilizer for the automated quantitative analysis of red blood cells, platelets, and with the addition of DxH ECO Lytic reagent, the differentiation of leukocytes subpopulations, and hemoglobin measurement.

DxH ECO Diluent is an osmotically balanced, pH neutral solution of organic buffers, germicides, and sodium/potassium salts. The diluent acts as an electrolyte and cell volume stabilizer for the automated quantitative analysis of red blood cells, platelets, and with the addition of DxH ECO Lytic reagent, the differentiation of leukocytes subpopulations, and hemoglobin measurement.

DxH ECO Cell Lyse is a cyanide-free reagent that measures hemoglobin by the oxyhemoglobin method. Surfactants are used to lyse the erythrocytesand release the hemoglobin. The released oxyhemoglobin reacts with an antioxidant and a stabilizing reagent, converting the oxyhemoglobin into a stablehemochromogen, which is photometrically measured by the instrument. The lytic reagent also solubilizes the red blood cell membrane while simultaneouslypreserving the white blood cell and NRBC cellular morphology to be counted and sized.

Access Thyroglobulin assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of thyroglobulin levels in human serum and plasma using the Access Immunoassay Systems. This device is intended to aid in monitoring for the presence of persistent or recurrent/metastatic disease in patients whohave differentiated thyroid cancer (DTC) and have had thyroid surgery (with or without ablative therapy), and who lack serum thyroglobulin antibodies.

The Access NT-proBNP assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of N-terminal pro B-type natriuretic peptide levels in human serum and plasma using the automated DxI Access Immunoassay Analyzers to aid in the following:1. diagnosis of patients suspected of having acute heart failure in the Emergency Department2. assessment of heart failure severity3. risk stratification of patients with heart failure4. risk stratification of patients with acute coronary syndrome

The Access NT-proBNP Calibrators are intended to calibrate the Access NT-proBNP assay for the quantitative determination of N-terminal pro B-type natriuretic peptide levels in human serum and plasma using the DxI Access Immunoassay Analyzers.

The Access Free T4 assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of free thyroxine levels in human serum and plasma (heparin) for the diagnosis and treatment of thyroid diseases using the Access Immunoassay Systems.

The Access Progesterone II assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of progesterone levels in human serum and plasma (lithium heparin) using the automated Access 2 Immunoassay System and DxI 9000 Access Immunoassay Analyzer. Measurements obtained by this deviceare used in the diagnosis and treatment of disorders of the ovaries or placenta.

The Access Progesterone II Calibrators are intended to calibrate the Access Progesterone II assay for the quantitative determination of progesterone levels in human serum and plasma (lithium heparin) on the automated Access 2 Immunoassay System and DxI 9000 Access Immunoassay Analyzer.

The Access Progesterone II Sample Diluent is intended for use with the Access Progesterone II assay to dilute samples containing progesterone concentrations greater than the S5 calibrator on the automated Access 2 Immunoassay System and DxI 9000 Access Immunoassay Analyzer.

The Access Thyroglobulin Antibody II assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of thyroglobulin antibody levels in human serum and plasma using the Access Immunoassay Systems. The measurement of thyroid autoantibodies may aid in the diagnosis of Hashimoto's disease, nontoxic goiter, and Graves' disease.

The Access CK-MB assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of CK-MB levels in human serum and plasma using the Access Immunoassay Systems to aid in the diagnosis and treatment of myocardial infarction and muscle diseases such as progressive, Duchenne-type muscular dystrophy.

MicroScan LabPro v5.00 Data Delivery-03, Electronic

LabPro V4_V5 Maintenance Update 05 (US), Electronic

DVD, LabPro V4_V5 Maintenance Update 05

PK7300

Wash Solution

ALP

α-Amylase

Calcium Arsenazo

D-Dimer

Uric Acid

Cytofuge® 2 Cytocentrifuge System