Reagent, Coronavirus Serological
Main Filters
Reagent, Coronavirus Serological
Abbott Ireland Diagnostics | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
06S6030 | 0 | - | ||
06S6101 | 0 | - | ||
06S6110 | 0 | - | ||
06S6120 | 0 | - | ||
06S6130 | 0 | - |
ACON LABORATORIES, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
200979 | 0 | - |
AGILENT TECHNOLOGIES, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
K1919 | 0 | - |
ASSURE TECH. (HANGZHOU) CO., LTD. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
1.0 | 0 | - |
Beckman Coulter, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
C58957 | 0 | - | ||
C58958 | 0 | - | ||
C58959 | 0 | - | ||
C58961 | 0 | - | ||
C58963 | 0 | - | ||
C58964 | 0 | - | ||
C69057 | 0 | - | ||
C69058 | 0 | - | ||
C69059 | 0 | - |
Biohit Healthcare (Hefei) Co., Ltd. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
REF:207.01.25.02 | 0 | - |
BTNX Inc | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
COV-13C25 | 0 | - |
DIASORIN SPA | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
311460 | 0 | - |
EUROIMMUN Medizinische Labordiagnostika AG | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
EI 2606-9601 A | 0 | - | ||
EI 2606-9601 G | 0 | - | ||
EI 2606-9601-20 G | 0 | - |
IMMUNODIAGNOSTIC SYSTEMS LIMITED | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
IS-ID6502 | 0 | - |
INBIOS INTERNATIONAL, INC | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
COVE-G | 0 | - | ||
COVE-M | 0 | - | ||
COVG-RE | 0 | - | ||
COVN-E | 0 | - |
LUMIQUICK DIAGNOSTICS, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
71108B | 0 | - |
NanoEnTek, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
FIC-COALQ | 0 | - | ||
FRCOA 020 | 0 | - |
ORTHO CLINICAL DIAGNOSTICS | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
6199919 | 0 | - | ||
6199920 | 0 | - | ||
6199921 | 0 | - | ||
6199922 | 0 | - | ||
6199923 | 0 | - | ||
6199924 | 0 | - | ||
6199960 | 0 | - | ||
6199961 | 0 | - |
ORTHO-CLINICAL DIAGNOSTICS, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
6199975 | 0 | - | ||
6199976 | 0 | - |
Phadia AB | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
83-0042-11 | 0 | - | ||
DECC066630 | 0 | - |
QUALIGEN INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
25000085 | 0 | - |
Siemens Healthcare Diagnostics Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
K7414 | 0 | - | ||
K7771 | 0 | - | ||
KC813 | 0 | - | ||
KC815 | 0 | - | ||
RF812 | 0 | - | ||
RF870 | 0 | - |
69 Results
Results Per Page
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Catalog #
Available
Starting At
Name
Company Name
Description
0
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QuickProfile™ 2019-nCoV IgG/IgM Antibody Test
LUMIQUICK DIAGNOSTICS, INC.
QuickProfile™ 2019-nCoV IgG/IgM Test Card is an immunochromatography based one step in vitro test. It is designed for the rapid qualitative determination of IgG and IgM antibodies to the 2019 novel coronavirus (2019-nCoV, SARS-CoV-2) in human serum, plasma, or whole blood. QuickProfile™ 2019-nCoV IgG/IgM Test Card is a supplemental rapid screening tool for symptomatic or asymptomatic carriers of the virus.
0
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Access SARS-CoV-2 IgG II QC
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgG II QC is intended for monitoring system performance of the Access SARS-CoV-2 IgG II assay using the Access Immunoassay Systems only.The Access SARS-CoV-2 IgG II QC are only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgG II Calibrator
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgG II Calibrators are intended to calibrate the Access SARS-CoV-2 IgG II assay for the in vitro semi-quantitative and qualitative detection of SARS-CoV-2 IgG antibodies in human plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, and sodium citrate) for use on the Access Immunoassay Systems only.The Access SARS-CoV-2 IgG II calibrators are only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgG II
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgG II assay is a paramagnetic particle, chemiluminescent immunoassay intended for the semi-quantitative and qualitative detection of IgG antibodies to SARS-CoV-2 in human plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, and sodium citrate). The Access SARS-CoV-2 IgG II assay is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity. The Access SARS-CoV-2 IgG II should not be used to diagnose or exclude acute SARS-CoV-2 infection. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests.The Access SARS-CoV-2 IgG II assay is only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgG QC
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgG QC is intended for monitoring system performance of the Access SARS-CoV-2 IgG assay. The Access SARS-CoV-2 IgG QC is for use on the Access Family of Immunoassay Systems only.The Access SARS-CoV-2 IgG QC are only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgG Calibrator
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgG Calibrators are intended to calibrate the Access SARS-CoV-2 IgG assay for the in vitro qualitative detection of SARS-CoV-2 IgG antibodies in human serum, serum separator tubes and plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, and sodium citrate) for use on the Access Family of Immunoassay Systems only. The Access SARS-CoV-2 IgG Calibrators are only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgG
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgG assay is a paramagnetic particle, chemiluminescent immunoassay intended for the qualitative detection of IgG antibodies to SARS-CoV-2 in human serum, serum separator tubes and plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, and sodium citrate). The Access SARS-CoV-2 IgG assay is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests.The Access SARS-CoV-2 IgG assay is only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgM QC
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgM QC is intended for monitoring system performance of the Access SARS-CoV-2 IgM assay. The Access SARS-CoV-2 IgM QC is for use on the Access Family of Immunoassay Systems only.The Access SARS-CoV-2 IgM QC are only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgM Calibrator
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgM Calibrators are intended to calibrate the Access SARS-CoV-2 IgM assay for the in vitro qualitative detection of SARS-CoV-2 IgM antibodies in human serum, serum separator tubes and plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, sodium citrate) for use on the Access Family of Immunoassay Systems only.The Access SARS-CoV-2 IgM calibrators are only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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Access SARS-CoV-2 IgM
Beckman Coulter, Inc.
The Access SARS-CoV-2 IgM is a paramagnetic particle, chemiluminescent immunoassay intended for the qualitative detection of IgM antibodies to SARS-CoV-2 in human serum, serum separator tubes and plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, sodium citrate). The Access SARS-CoV-2 IgM is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity. The Access SARS-CoV-2 IgM should not be used to diagnose acute SARS-CoV-2 infection. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity tests.The Access SARS-CoV-2 IgM assay is only for use under the Food and Drug Administration's Emergency Use Authorization.
0
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VITROS
ORTHO-CLINICAL DIAGNOSTICS, INC.
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Calibrators
0
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VITROS
ORTHO-CLINICAL DIAGNOSTICS, INC.
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Reagent Pack
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-COV-2 IgG Quantitative Calibrator
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-COV-2 IgG Quantitative Reagent Pack
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total Controls
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total Calibrator
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total Reagent Pack
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Controls
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Calibrator
0
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VITROS
ORTHO CLINICAL DIAGNOSTICS
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Reagent Pack
0
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FREND
NanoEnTek, Inc.
The COVID-19 total Ab is designed for the qualitative and quantitative measurement of anti-coronavirus IgG and IgM in human serum and plasma (Li-heparinized, EDTA,and citrate) by fluorescence immunoassay (FIA) using the FREND™ System.
0
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FREND
NanoEnTek, Inc.
The COVID-19 total Ab Control LQ is designed to estimate the test and FREND™ COVID-19 total Ab cartridges. COVID-19 total Ab Control LQ is not intended for use as a standard.
0
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ACON SARS-CoV-2 IgG/IgM Rapid Test
ACON LABORATORIES, INC.
Test Cassettes (25), 2.5mL Buffer Bottles (2), Droppers (25)
0
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DV/DM COV2T/CV2T POS/NEG CTRL
Siemens Healthcare Diagnostics Inc.
DV/DM COV2T/CV2T POS/NEG CTRL
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