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.

The Access Ferritin Calibrators are intended to calibrate the Access Ferritin assay for the quantitative determination of ferritin levels in human serum and plasma (heparin) using the Access Immunoassay Systems.

The Access CEA assay is a paramagnentic particle, chemiluminescent immunoassay for the quantitative determination of Carcinoembryonic Antigen (CEA) levels in human serum, using the Access Immunoassay Systems.

The Access CEA Calibrators (BSA matrix) are intended to calibrate the Access CEA assay for the quantitative determination of Carcinoembryonic Antigen (CEA) levels in human serum, using the Access Immunoassay Systems.

The Access CEA Diluent (BSA matrix) is intended for use with the Access CEA assay to dilute patient samples containing CEA concentrations greater than the Access CEA Calibrator S5

The Access CEA QC (BSA matrix) controls are intended for monitoring the system performance of immunoenzymatic procedures for the quantitative measurement of Carcinoembryonic Antigen (CEA) using Access CEA reagents.

The 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.

High Sensitivity Cardiac C-Reactive Protein Reagent (CRPH 2 x 200)

The Access OV Monitor assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of CA 125 antigen levels in human serum and plasma using the Access Immunoassay Systems.

The Access OV Monitor Calibrators are intended to calibrate the Access OV Monitor assay for the quantitative determination of CA 125 antigen levels in human serum and plasma using the Access Immunoassay Systems.

The Access BR Monitor assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of CA 15-3 antigen levels in human serum and plasma (heparin) using the Access Immunoassay Systems.

The Access GI Monitor assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of CA 19-9 antigen levels in human serum and plasma using the Access Immunoassay Systems.

Icon Mono, 30 Test Box

IMMAGE Immunochemistry Systems KAP Kappa Light Chain Reagent

IMMAGE Immunochemistry Systems C3 Complement C3 Reagent

IMMAGE Immunochemistry Systems IGA Immunoglobulin A Reagent

IMMAGE Immunochemistry Systems LAM Lambda Light Chain Reagent

IMMAGE Immunochemistry Systems HPT Haptoglobin Reagent

IMMAGE Immunochemistry Systems C4 Complement C4 Reagent

IMMAGE Immunochemistry Systems CRP C-Reactive Protein Reagent

IMMAGE Immunochemistry Systems PAB Prealbumin Reagent

Immunoglobulin A Reagent (Ig-A 2 x 150)

Immunoglobulin G Reagent (Ig-G 2 x 150)

Immunoglobulin M Reagent (Ig-M 2 x 150)

Transferrin Reagent (TRFN 2 x 150)

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

C3 Reagent (C3 2 x 100)

C4 Reagent (C4 2 x 100)

Urine CSF Albumin

Total Immunoglobulin E (IgE) Reagent kit for AU/DxC AU clinical chemistry analyzers.

SP RF Direct Slide Test 100 Determination

Rheumatoid Factor Test Slide CLIA Non-Waived

Mono Rapid Test

Aptima® Trichomonas vaginalis Controls Kit.

Aptima® Trichomonas vaginalis Assay, 250 test, box 1 of 2 (2°C to 8°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Tigris® DTS® System.

Aptima® Trichomonas vaginalis Assay, 250 test, box 2 of 2 (15°C to 30°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Tigris® DTS® System.

Aptima® Trichomonas vaginalis Assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Tigris® DTS® System.

Aptima® Trichomonas vaginalis Assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Tigris® DTS® System.

Aptima® Trichomonas vaginalis Assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Panther® System.

Aptima® Trichomonas vaginalis Assay, 250 test, box 2 of 2 (15°C to 30°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Panther® System.

Aptima® Trichomonas vaginalis Assay, 250 test, box 1 of 2 (2°C to 8°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Panther® System.

Aptima® Trichomonas vaginalis Assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima® Trichomonas vaginalis Assay is an in vitro qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Panther® System.

TEST KIT, MONO WAIVED APPRV F/

30 Test Ported TPSA Immunoassay Kit