Other products from "EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 04049016045403 FA 1522-2010 DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control 2 ANA IFA: HEp-20-10
2 04049016045397 FA 1522-2005 ANA IFA: HEp-20-10
3 04049016045380 FA 1522-2003 DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control 2 ANA IFA: HEp-20-10
4 04049016145745 MP 2606-0200 QJR Reagents, 2019-Novel Coronavirus Nucleic Acid EURORealTime SARS-CoV-2
5 04049016145691 MP 2606-0100 QJR Reagents, 2019-Novel Coronavirus Nucleic Acid EURORealTime SARS-CoV-2
6 04049016145660 MP 2606-0425 QJR Reagents, 2019-Novel Coronavirus Nucleic Acid EURORealTime SARS-CoV-2
7 04049016145653 MP 2606-0225 QJR Reagents, 2019-Novel Coronavirus Nucleic Acid EURORealTime SARS-CoV-2
8 04049016145646 MP 2606-0125 QJR Reagents, 2019-Novel Coronavirus Nucleic Acid EURORealTime SARS-CoV-2
9 04049016114895 EI 2132-9601-24 O LSR Reagent, Borrelia Serological Reagent 2 Lyme ELISA (IgG/IgM)
10 04049016109723 YG 0153-0101 JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use 1 EUROBlotOne
11 04049016109709 YG 0033-0101-5 JQW Station, Pipetting And Diluting, For Clinical Use 1 Sprinter XL (model 160 samples, IFA)
12 04049016109693 YG 0033-0101-4 JQW Station, Pipetting And Diluting, For Clinical Use 1 Sprinter XL (model 160 samples, IFA incl. incubator)
13 04049016109679 YG 0033-0101-26 JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use 1 Sprinter XL (model 240 samples, IFA/ELISA)
14 04049016096047 EI 2050-9601 M GOX Antigen, B. Pertussis 1 Anti-Bordetella pertussis ELISA (IgM)
15 04049016092575 FA 112d-2010-51 OSK Anti-Glutamate Receptor (Type Nmda) Ifa 2 Anti-Glutamate receptor (type NMDA) IFA
16 04049016092568 FA 112d-2005-51 OSK Anti-Glutamate Receptor (Type Nmda) Ifa 2 Anti-Glutamate receptor (type NMDA) IFA
17 04049016092551 FA 112d-1010-51 OSK Anti-Glutamate Receptor (Type Nmda) Ifa 2 Anti-Glutamate receptor (type NMDA) IFA
18 04049016092544 FA 112d-1005-51 OSK Anti-Glutamate Receptor (Type Nmda) Ifa 2 Anti-Glutamate receptor (type NMDA) IFA
19 04049016092537 FA 112d-1003-51 OSK Anti-Glutamate Receptor (Type Nmda) Ifa 2 Anti-Glutamate receptor (type NMDA) IFA
20 04049016091608 EA 1502-4801-1 G OEG Autoantibodies, Skin (Bullous Pemphigoid 180 And Bullous Pemphigoid 230 2 Anti-BP230-CF ELISA (IgG)
21 04049016091288 FA 1201-2010-32 MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca) 2 EUROPLUS Granulocyte Mosaic 32
22 04049016091271 FA 1201-2005-32 MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca) 2 EUROPLUS Granulocyte Mosaic 32
23 04049016091264 FA 1201-1010-32 MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca) 2 EUROPLUS Granulocyte Mosaic 32
24 04049016091257 FA 1201-1005-32 MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca) 2 EUROPLUS Granulocyte Mosaic 32
25 04049016091240 FA 1201-1003-32 MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca) 2 EUROPLUS Granulocyte Mosaic 32
26 04049016089193 EA 1496-4801 G NBO Autoantibodies,Skin(Desmoglein 1 And Desmoglein 3) 2 Anti-Desmoglein 3 ELISA (IgG)
27 04049016089186 EA 1495-4801 G NBO Autoantibodies,Skin(Desmoglein 1 And Desmoglein 3) 2 Anti-Desmoglein 1 ELISA (IgG)
28 04049016086017 EA 1590-9601-9 G LLL Extractable Antinuclear Antibody, Antigen And Control 2 Anti-ENA Pool ELISA (IgG)
29 04049016085478 DN 2050-24001 G GOX Antigen, B. Pertussis 1 EUROLINE Bordetella pertussis (IgG)
30 04049016085447 DN 2050-1601 G GOX Antigen, B. Pertussis 1 EUROLINE Bordetella pertussis (IgG)
31 04049016068822 YG 0151-0101 JQW Station, Pipetting And Diluting, For Clinical Use 1 EUROBlotMaster
32 04049016067887 FI 2861-2005 M LSG Candida Species, Antibody Detection 2 Anti-Candida albicans IFA (IgM)
33 04049016067870 FI 2861-1010 M LSG Candida Species, Antibody Detection 2 Anti-Candida albicans IFA (IgM)
34 04049016067863 FI 2861-1005 M LSG Candida Species, Antibody Detection 2 Anti-Candida albicans IFA (IgM)
35 04049016067856 FI 2861-1003 M LSG Candida Species, Antibody Detection 2 Anti-Candida albicans IFA (IgM)
36 04049016045366 FA 1522-1050 DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control 2 ANA IFA: HEp-20-10
37 04049016045359 FA 1522-1010 DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control 2 ANA IFA: HEp-20-10
38 04049016045342 FA 1522-1005 DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control 2 ANA IFA: HEp-20-10
39 04049016045335 FA 1522-1003 DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control 2 ANA IFA: HEp-20-10
40 04049016035930 EV 3011-9601 A MST Antibodies, Gliadin 2 Anti-Gliadin (GAF-3X) ELISA (IgA)
41 04049016028369 EI 2721-9601-1 A GQT Antisera, Cf, Parainfluenza Virus 1-4 1 Anti-Parainfluenza Viruses Pool ELISA (IgA)
42 04049016028321 EI 2691-9601-1 G GNS Antisera, Hai, Influenza Virus A, B, C 1 Anti-Influenza A/B Virus Pool ELISA (IgG)
43 04049016027560 EI 2189-9601 G GSM Antisera, Fluorescent, Brucella Spp. 2 Anti-Brucella abortus ELISA (IgG)
44 04049016027522 EI 2150-9601 M MJH Legionella, Spp., Elisa 2 Anti-Legionella pneumophila ELISA (IgM)
45 04049016134992 DY 2133-24001-1 M LSR Reagent, Borrelia Serological Reagent 2 Anti-Borrelia burgdorferi US EUROLINE-WB (IgM)
46 04049016134985 DY 2133-3001-1 M LSR Reagent, Borrelia Serological Reagent 2 Anti-Borrelia burgdorferi US EUROLINE-WB (IgM)
47 04049016119999 FC 1911-0010 A MVM Autoantibodies, Endomysial(Tissue Transglutaminase) 2 IFA: Oesophagus (Monkey) IgA EUROPattern
48 04049016119982 FC 1911-2010 A MVM Autoantibodies, Endomysial(Tissue Transglutaminase) IFA: Oesophagus (Monkey) IgA EUROPattern
49 04049016119975 FC 1911-2005 A MVM Autoantibodies, Endomysial(Tissue Transglutaminase) 2 IFA: Oesophagus (Monkey) IgA EUROPattern
50 04049016119968 FC 1911-1010 A MVM Autoantibodies, Endomysial(Tissue Transglutaminase) 2 IFA: Oesophagus (Monkey) IgA EUROPattern
Other products with the same Product Code "QKO"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00682607200979 L031-11711 200979 Test Cassettes (25), 2.5mL Buffer Bottles (2), Droppers (25) ACON SARS-CoV-2 IgG/IgM Rapid Test ACON LABORATORIES, INC.
2 00630414607139 11417771 K7771 Vista COV2G Assay Vista COV2G Assay SIEMENS HEALTHCARE DIAGNOSTICS INC.
3 00630414607030 11417770 RF870 Dimension CV2G Assay Dimension CV2GAssay SIEMENS HEALTHCARE DIAGNOSTICS INC.
4 00630414605500 11417414 K7414 Vista COV2T Assay Vista COV2T Assay SIEMENS HEALTHCARE DIAGNOSTICS INC.
5 00630414605494 11417413 KC813 DV/DM COV2T/CV2T CAL DV/DM COV2T/CV2T CAL SIEMENS HEALTHCARE DIAGNOSTICS INC.
6 00630414605425 11417415 KC815 DV/DM COV2T/CV2T POS/NEG CTRL DV/DM COV2T/CV2T POS/NEG CTRL SIEMENS HEALTHCARE DIAGNOSTICS INC.
7 00630414605418 11417412 RF812 Dimension CV2T Assay Dimension CV2T Assay SIEMENS HEALTHCARE DIAGNOSTICS INC.
8 00380740193867 06S6130 06S6130 AdviseDx SARS-CoV-2 IgG II Reagent Kit 1000 Test Alinity ABBOTT IRELAND DIAGNOSTICS
9 00380740193843 06S6120 06S6120 AdviseDx SARS-CoV-2 IgG II Reagent Kit 200 Test Alinity ABBOTT IRELAND DIAGNOSTICS
10 00380740193829 06S6110 06S6110 AdviseDx SARS-CoV-2 IgG II Control Kit Alinity ABBOTT IRELAND DIAGNOSTICS
11 00380740193805 06S6101 06S6101 AdviseDx SARS-CoV-2 IgG II Calibrator Kit Alinity ABBOTT IRELAND DIAGNOSTICS
12 00380740193782 06S6030 06S6030 AdviseDx SARS-CoV-2 IgG II Reagent Kit 500 Test ARCHITECT ABBOTT IRELAND DIAGNOSTICS
13 00380740193768 06S6020 06S6020 AdviseDx SARS-CoV-2 IgG II Reagent Kit 100 Test ARCHITECT ABBOTT IRELAND DIAGNOSTICS
14 00380740193744 06S6010 06S6010 AdviseDx SARS-CoV-2 IgG II Control Kit ARCHITECT ABBOTT IRELAND DIAGNOSTICS
15 00380740193720 06S6001 06S6001 AdviseDx SARS-CoV-2 IgG II Calibrator Kit ARCHITECT ABBOTT IRELAND DIAGNOSTICS
16 00380740192167 06R8730 06R8730 AdviseDx SARS-CoV-2 IgM Reagent Kit 500 Test ARCHITECT ABBOTT IRELAND DIAGNOSTICS
17 00380740192150 06R8630 06R8630 SARS-CoV-2 IgG Reagent Kit 500 Tests ARCHITECT ABBOTT LABORATORIES
18 00380740192136 06R9030 06R9030 SARS-CoV-2 IgG Reagent Kit 1000 Tests Alinity ABBOTT LABORATORIES
19 00380740192129 06R9020 06R9020 SARS-CoV-2 IgG Reagent Kit 200 Tests Alinity ABBOTT LABORATORIES
20 00380740192112 06R9010 06R9010 SARS-CoV-2 IgG Control Kit Alinity ABBOTT LABORATORIES
21 00380740192105 06R9001 06R9001 SARS-CoV-2 IgG Calibrator Kit Alinity ABBOTT LABORATORIES
22 00380740192099 06R9130 06R9130 AdviseDx SARS-CoV-2 IgM Reagent Kit 1000 Test Alinity ABBOTT IRELAND DIAGNOSTICS
23 00380740192082 06R9120 06R9120 AdviseDx SARS-CoV-2 IgM Reagent Kit 200 Test Alinity ABBOTT IRELAND DIAGNOSTICS
24 00380740192075 06R9110 06R9110 AdviseDx SARS-CoV-2 IgM Control Kit Alinity ABBOTT IRELAND DIAGNOSTICS
25 00380740192068 06R9101 06R9101 AdviseDx SARS-CoV-2 IgM Calibrator Kit Alinity ABBOTT IRELAND DIAGNOSTICS
26 00380740191863 06R8720 06R8720 AdviseDx SARS-CoV-2 IgM Reagent Kit 100 Test ARCHITECT ABBOTT IRELAND DIAGNOSTICS
27 00380740191856 06R8710 06R8710 AdviseDx SARS-CoV-2 IgM Control Kit ARCHITECT ABBOTT IRELAND DIAGNOSTICS
28 00380740191849 06R8701 06R8701 AdviseDx SARS-CoV-2 IgM Calibrator Kit ARCHITECT ABBOTT IRELAND DIAGNOSTICS
29 00380740191832 06R8620 06R8620 SARS-CoV-2 IgG Reagent Kit 100 Tests ARCHITECT ABBOTT LABORATORIES
30 00380740191825 06R8610 06R8610 SARS-CoV-2 IgG Control Kit ARCHITECT ABBOTT LABORATORIES
31 00380740191818 06R8601 06R8601 SARS-CoV-2 IgG Calibrator Kit ARCHITECT ABBOTT LABORATORIES
32 M90171108B0 71108B 71108B QuickProfile™ 2019-nCoV IgG/IgM Test Card is an immunochromatography based one s 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. QuickProfile™ 2019-nCoV IgG/IgM Antibody Test LUMIQUICK DIAGNOSTICS, INC.
33 15099590742768 C69059 C69059 The Access SARS-CoV-2 IgG II QC is intended for monitoring system performance of 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. Access SARS-CoV-2 IgG II QC BECKMAN COULTER, INC.
34 15099590742751 C69058 C69058 The Access SARS-CoV-2 IgG II Calibrators are intended to calibrate the Access SA 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. Access SARS-CoV-2 IgG II Calibrator BECKMAN COULTER, INC.
35 15099590742744 C69057 C69057 The Access SARS-CoV-2 IgG II assay is a paramagnetic particle, chemiluminescent 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. Access SARS-CoV-2 IgG II BECKMAN COULTER, INC.
36 15099590738662 C58964 C58964 The Access SARS-CoV-2 IgG QC is intended for monitoring system performance of th 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. Access SARS-CoV-2 IgG QC BECKMAN COULTER, INC.
37 15099590738655 C58963 C58963 The Access SARS-CoV-2 IgG Calibrators are intended to calibrate the Access SARS- 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. Access SARS-CoV-2 IgG Calibrator BECKMAN COULTER, INC.
38 15099590738648 C58961 C58961 The Access SARS-CoV-2 IgG assay is a paramagnetic particle, chemiluminescent imm 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. Access SARS-CoV-2 IgG BECKMAN COULTER, INC.
39 15099590738631 C58959 C58959 The Access SARS-CoV-2 IgM QC is intended for monitoring system performance of th 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. Access SARS-CoV-2 IgM QC BECKMAN COULTER, INC.
40 15099590738624 C58958 C58958 The Access SARS-CoV-2 IgM Calibrators are intended to calibrate the Access SARS- 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. Access SARS-CoV-2 IgM Calibrator BECKMAN COULTER, INC.
41 15099590738617 C58957 C58957 The Access SARS-CoV-2 IgM is a paramagnetic particle, chemiluminescent immunoass 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. Access SARS-CoV-2 IgM BECKMAN COULTER, INC.
42 10816467020386 SARS-CoV-2 IgG Immunoassay 25000085 90 Test Kit SARS-CoV-2 IgG Immunoassay FastPack SARS-CoV-2 IgG QUALIGEN INC.
43 10758750034581 6199976 6199976 VITROS Immunodiagnostic Products Anti-SARS-CoV-2 Total N Antibody Calibrators VITROS ORTHO-CLINICAL DIAGNOSTICS, INC.
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