Other products from "BIO-RAD LABORATORIES, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00847865013178 26203 26203 Anti-HBc IgM EIA, Cutoff Calibrator, 1.5 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
2 00847865013161 26202 26202 Anti-HBc IgM EIA, Conjugate, Lyophilized, 7.5 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
3 00847865013154 26201 26201 Anti-HBc IgM EIA, Negative Control, 0.8 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
4 00847865013147 26200 26200 Anti-HBc IgM EIA, Positive Control,1.6 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
5 00847865013130 26199 26199 Anti-HBc IgM EIA, Specimen Diluent, 30 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
6 00847865013123 26198 26198 Anti-HBc IgM EIA Conjugate Diluent, 30 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
7 00847865013116 26197 26197 Anti-HBc EIA, Negative Control, 0.8 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
8 00847865013109 26196 26196 Anti-HBc EIA, Specimen Diluent, 30 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
9 00847865013093 26195 26195 Anti-HBc EIA, Cutoff Calibrator, 1.5 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
10 00847865013086 26194 26194 Anti-HBc EIA, Positive Control, 0.8 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
11 00847865013079 26193 26193 Anti-HBc EIA, Conjugate Reagent 30 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
12 00847865011372 26186 26186 MONOLISA™ Anti-HBc EIA 192 Tests LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
13 00847865011365 26174 26174 MONOLISA™ Anti-HBc IgM EIA, 192 Tests LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
14 00847865002110 26156 26156 Anti-HBs EIA, Specimen Diluent 10 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
15 00847865002103 26155 26155 Anti-HBs EIA, Conjugate Diluent 15 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
16 00847865002097 26154 26154 Anti-HBs EIA, 10 mIU/mL Calibrator 1.8 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
17 00847865002080 26153 26153 Anti-HBs EIA, Negative Control 1.5 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
18 00847865002073 26152 26152 Anti-HBs EIA, Positive Control 1.5 mL LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
19 00847865002066 26151 26151 Anti-HBs EIA Hepatitis B Surface Antigen (Human) Horeseradish Peroxidase Conjugate LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
20 00847865002042 25219 25219 MONOLISA™ Anti-HBs EIA Calibrator Kit LOM Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm) 3 MONOLISA™
21 00847865001687 31996 31996 Kallestad Patient Sample Diluent DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
22 00847865001670 26106 26106 Kallestad HEp-2 Cell Line 24 Well Slides DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
23 00847865001779 30480 30480 Kallestad FITC Conjugate DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
24 00847865001762 30446 30446 Kallestad FITC Conjugate DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
25 00847865001755 30431 30431 Kallestad Evans' Blue Counterstain DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
26 00847865001724 26115 26115 Kallestad Mouse Stomach/Kidney 8 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
27 00847865001717 26112 26112 Kallestad Mouse Stomach/Kidney 8 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
28 00847865001700 26111 26111 Kallestad Mouse Stomach/Kidney 8 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
29 00847865001694 30443 30443 Kallestad Mouse Stomach Kidney Substrate DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
30 00847865001656 26104 26104 Kallestad HEp-2 Cell Line 12 Well Slides DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
31 00847865001649 26103 26103 Kallestad HEp-2 Cell Line 12 Well Slides DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
32 00847865001632 26102 26102 Kallestad HEp-2 Cell Line 12 Well Slides DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
33 00847865001625 26101 26101 Kallestad HEp-2 Cell Line 6 Well Slides DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
34 00847865001618 26100 26100 Kallestad HEp-2 Cell Line 6 Well Slides DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
35 00847865001601 30472 30472 Kallestad HEp-2 Cell Line Substrate DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
36 00847865001595 30471 30471 Kallestad HEp-2 Cell Line Substrate DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
37 00847865001588 32583 32583 Kallestad HEp-2 Cell Line Substrate DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
38 00847865001571 26110 26110 Kallestad Crithidia luciliae 8 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
39 00847865001564 26109 26109 Kallestad Crithidia luciliae 8 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
40 00847865001557 26108 26108 Kallestad Crithidia luciliae 4 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
41 00847865001540 26107 26107 Kallestad Crithidia luciliae 4 Well Slides DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
42 00847865001533 31069 31069 Kallestad Crithidia luciliae Substrate DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
43 00847865001526 30404 30404 Kallestad Crithidia luciliae Substrate DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
44 00847865001496 32514 32514 MONOFLUO Legionella pneumophila IFA Test Kit LHL REAGENTS, ANTIBODY, LEGIONELLA, DIRECT & INDIRECT FLUORESCENT 2 Kallestad
45 00847865001205 30403 30403 Kallestad Mounting Media DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Kallestad
46 00847865019347 12000667 12000667 Slide Blotters, 8-well DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Bio-Rad Laboratories, Inc.
47 00847865019354 12000668 12000668 Slide Blotters, 24-well DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Bio-Rad Laboratories, Inc.
48 00847865019330 12000666 12000666 Slide Blotters, 4-well DHN ANTINUCLEAR ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Bio-Rad Laboratories, Inc.
49 00847865017343 12000660 12000660 Slide Blotters, 6-well DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Bio-Rad Laboratories, Inc.
50 00847865017244 12000661 12000661 Slide Blotters, 12-well DBM ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL 2 Bio-Rad Laboratories, Inc.
Other products with the same Product Code "MZF"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00608337103403 1001-0340 OraQuick In Home HIV Test ORASURE TECHNOLOGIES, INC.
2 00608337001334 1001-0528 OraQuick In Home HIV Test, Pharmacy ORASURE TECHNOLOGIES, INC.
3 00608337000962 1001-0374 OraQuick In Home HIV Test (Not for Resale) ORASURE TECHNOLOGIES, INC.
4 00607158000083 65-9502-0 The DPP® HIV-Syphilis is a single-use rapid, qualitative, multiplex, immunoassay The DPP® HIV-Syphilis is a single-use rapid, qualitative, multiplex, immunoassay for the detection of antibodies to Human Immunodeficiency Virus Types 1 and 2 (HIV-1/2), and/or Treponema pallidum bacteria (the causative agent of syphilis) in fingerstick whole blood, potassium-EDTA venous whole blood or potassium-EDTA plasma specimens. The test is intended to be used with the DPP Micro Reader. The test is intended for use by trained professionals in point of care and laboratory settings to aid in the diagnosis of HIV and syphilis infection. DPP HIV-Syphilis CHEMBIO DIAGNOSTIC SYSTEMS INC.
5 00607158000076 60-9549-0 The Chembio HIV Reactive/Nonreactive Controls are quality control reagents for u The Chembio HIV Reactive/Nonreactive Controls are quality control reagents for use with the Chembio HIV 1/2 STAT-PAK® Assay only. Chembio HIV Reactive/Nonreactive Controls are human, plasma-based reagents. The Controls are specifically formulated and manufactured to ensure performance of the test, and are used to verify the user’s ability to properly perform the test and interpret the results. Each HIV Rapid Test Control Pack contains a Product Insert and three Vials (one HIV 1 Reactive Control, one HIV 2 Reactive Control and one Nonreactive Control).One Vial containing 0.25 mL of heat inactivated human plasma positive for antibodies to HIV-1, diluted in normal human plasma. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies.One Vial containing 0.25 mL of heat inactivated human plasma positive for antibodies to HIV-2, diluted in normal human plasma. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies.One Vial containing 0.25 mL of normal human plasma negative for antibodies to HIV-1 and HIV-2. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies. Chembio HIV Reactive/Nonreactive Controls CHEMBIO DIAGNOSTIC SYSTEMS INC.
6 00607158000069 60-9507-0 The Chembio SURE CHECK® HIV 1/2 Assay is a single-use immunochromatographic test The Chembio SURE CHECK® HIV 1/2 Assay is a single-use immunochromatographic test for the detection of antibodies to Human Immunodeficiency Virus Types 1 (HIV-1) and Type 2 (HIV-2) in fingerstick whole blood, venous whole blood, and serum or plasma specimens. The Chembio SURE CHECK® HIV 1/2 Assay is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1 and HIV-2. This test is suitable for use in multi-test algorithms designed for the statistical validation of rapid HIV test results. When multiple rapid HIV tests are available, this test should be used in appropriate multi-test algorithms. Each kit contains 25 individually pouched tests each containing 1 Sampler with a Test Strip inside, 1 Buffer Vial attached to the Sampler (~350μL), 1 Sterile Safety Lancet, 1 Bandage, 1 Desiccant Packet; 25 Disposable Test Stands; 1 Product Insert; 25 Copies of Subject Information Notice. Chembio SURE CHECK HIV 1/2 Assay CHEMBIO DIAGNOSTIC SYSTEMS INC.
7 00607158000052 60-9505-1 The Chembio HIV 1/2 STAT-PAK® Assay is a single-use immunochromatographic test f The Chembio HIV 1/2 STAT-PAK® Assay is a single-use immunochromatographic test for the detection of antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) in fingerstick whole blood, venous whole blood, serum or plasma specimens. The Chembio HIV 1/2 STAT-PAK® assay is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1 and HIV-2. This test is suitable for use in multi-test algorithms designed for the statistical validation of rapid HIV test results. When multiple rapid HIV tests are available, this test should be used in appropriate multi-test algorithms. Each kit contains 20 individually pouched tests, 1 bottle of HIV Running Buffer, 20 Disposable Loops, 1 Product Insert, and 20 Copies of Subject Information Notice. Chembio HIV 1/2 Stat-Pak Assay CHEMBIO DIAGNOSTIC SYSTEMS INC.
8 00607158000045 60-9552-0 The Chembio HIV Reactive/Nonreactive Controls are quality control reagents for u The Chembio HIV Reactive/Nonreactive Controls are quality control reagents for use with the Chembio DPP HIV 1/2 Assay only. Chembio HIV Reactive/Nonreactive Controls are human, plasma-based reagents. The Controls are specifically formulated and manufactured to ensure performance of the test, and are used to verify the user’s ability to properly perform the test and interpret the results. Each HIV Rapid Test Control Pack contains a Product Insert and three Vials (one HIV 1 Reactive Control, one HIV 2 Reactive Control and one Nonreactive Control) as described. One Vial containing 0.5mL of heat inactivated human plasma positive for antibodies to HIV-1, diluted in normal human plasma. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies.One Vial containing 0.5mL of heat inactivated human plasma positive for antibodies to HIV-2, diluted in normal human plasma. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies. One Vial containing 0.5mL of normal human plasma negative for antibodies to HIV-1 and HIV-2. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies. Chembio DPP HIV 1/2 Rapid Test Control Pack CHEMBIO DIAGNOSTIC SYSTEMS INC.
9 00607158000038 60-9546-0 The Clearview® HIV Reactive/Nonreactive Controls are quality control reagents fo The Clearview® HIV Reactive/Nonreactive Controls are quality control reagents for use with the Clearview® COMPLETE HIV 1/2 Assay only. Clearview® HIV Reactive/Nonreactive Controls are human, plasma-based reagents. The Controls are specifically formulated and manufactured to ensure performance of the test, and are used to verify the user’s ability to properly perform the test and interpret the results. Each HIV Rapid Test Control Pack contains a Product Insert and three Vials (one HIV 1 Reactive Control, one HIV 2 Reactive Control and one Nonreactive Control).One Vial containing 0.25 mL of heat inactivated human plasma positive for antibodies to HIV-1, diluted in normal human plasma. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies.One Vial containing 0.25 mL of heat inactivated human plasma positive for antibodies to HIV-2, diluted in normal human plasma. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies.One Vial containing 0.25 mL of normal human plasma negative for antibodies to HIV-1 and HIV-2. Negative for Hepatitis B surface antigen, Hepatitis C antibody and HTLV I/II antibodies. Clearview HIV Reactive/Nonreactive Controls CHEMBIO DIAGNOSTIC SYSTEMS INC.
10 00607158000021 60-9523-0 The Clearview® COMPLETE HIV 1/2 assay is a single-use immunochromatographic test The Clearview® COMPLETE HIV 1/2 assay is a single-use immunochromatographic test for the detection of antibodies to Human Immunodeficiency Virus Types 1 (HIV-1) and Type 2 (HIV-2) in fingerstick whole blood, venous whole blood, and serum or plasma specimens. The Clearview® COMPLETE HIV 1/2 assay is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1 and HIV-2. This test is suitable for use in multi-test algorithms designed for the statistical validation of rapid HIV test results. When multiple rapid HIV tests are available, this test should be used in appropriate multi-test algorithms. Each kit contains 25 individually pouched tests, 25 Disposable Test Stands, 1 Product Insert, and 25 Copies of Subject Information Notice. Clearview Complete HIV 1/2 CHEMBIO DIAGNOSTIC SYSTEMS INC.
11 00607158000007 65-9500-0 The Chembio DPP® HIV 1/2 Assay is a single-use immunochromatographic test for th The Chembio DPP® HIV 1/2 Assay is a single-use immunochromatographic test for the detection of antibodies to Human Immunodeficiency Virus Types 1 and 2 (HIV-1/2) in oral fluid, fingerstick whole blood, venous whole blood, serum, or plasma samples. The Chembio DPP HIV 1/2 Assay is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1 and HIV-2. This test is suitable for use in multi-test algorithms designed for the statistical validation of rapid HIV test results. When multiple rapid HIV tests are available, this test should be used in appropriate multi-test algorithms. Each kit contains 20 individually pouched tests, 1 bottle of DPP HIV Running Buffer, 20 Sampletainer Bottles, 20 Oral Fluid Swabs, 20 Disposable Loops, 1 Product Insert, and 20 Copies of Subject Information Notice. Chembio DPP HIV 1/2 Assay CHEMBIO DIAGNOSTIC SYSTEMS INC.
12 00380740146252 08P0702 08P0702 Alinity i HIV Ag/Ab Combo Calibrator Alinity ABBOTT GMBH
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14 00380740121778 08P0731 08P0731 Alinity i HIV Ag/Ab Combo Reagent Kit 1200 Tests Alinity ABBOTT GMBH
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28 10628451188152 815311007514 HIV-1 Antibody Test Controls (Test Controls) are external quality control agents HIV-1 Antibody Test Controls (Test Controls) are external quality control agents intended for use only with Reveal G4. HIV-1 Antibody Test Controls MEDMIRA LABORATORIES INC
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30 10628451188138 815311007538 Reveal G4 Rapid HIV-1 Antibody Test (Reveal G4) is a single use, qualitatitve im Reveal G4 Rapid HIV-1 Antibody Test (Reveal G4) is a single use, qualitatitve immunoassay to detect antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) in human whole blood (venipuncture and fingerstick), serum, and plasma. Reveal G4 is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1. This test is suitable for use in multi-test algorithms designed for statistical validation of rapid HIV test results. When multiple rapid tests are available, this test should be used in appropriate multi-test algorithms. Reveal G4 Rapid HIV-1 Antibody Test MEDMIRA LABORATORIES INC
31 10628451188121 815311007569 Reveal G4 Rapid HIV-1 Antibody Test (Reveal G4) is a single use, qualitatitve im Reveal G4 Rapid HIV-1 Antibody Test (Reveal G4) is a single use, qualitatitve immunoassay to detect antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) in human whole blood (venipuncture and fingerstick), serum, and plasma. Reveal G4 is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1. This test is suitable for use in multi-test algorithms designed for statistical validation of rapid HIV test results. When multiple rapid tests are available, this test should be used in appropriate multi-test algorithms. Reveal G4 Rapid HIV-1 Antibody Test MEDMIRA LABORATORIES INC
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33 10628451188107 815311007545 HIV-1 Antibody Test Controls (Test Controls) are external quality control agents HIV-1 Antibody Test Controls (Test Controls) are external quality control agents intended for use only with Reveal G4. HIV-1 Antibody Test Controls MEDMIRA LABORATORIES INC
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44 06865978010710 80-1071 80-1071 INSTI Test Controls HIV-1 INSTI Test Controls HIV-1 BIOLYTICAL LABORATORIES INC
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