SEARCH RESULTS FOR: 男M♥飞机号@zykaifa中国云南省普洱市墨江哈尼族自治县(41984 results)
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AccuDiag ™ Rubella IgM Enzyme- Linked Immunosorbent Assay (ELISA) is intended for the in vitro qualitative determination of IgM antibodies in human serum and as an aid in the diagnosis of current or recent infection with Rubella virus
Diagnostic Automation, Inc.
DACD1302-1
In Commercial Distribution
- 00850049545693 ()
- 96 tests
1302-1
- Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
The ZEUS ELISA Parvovirus B19 IgM Test System is intended for the qualitative detection of IgM class antibodies to human parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human parvovirus B19. The test is also for all symptomatic patients as an aid in the diagnosis of fifth disease (erythema infectiosum). This test is intended for in vitro diagnostic use only.
ZEUS SCIENTIFIC, INC.
SM9Z7701M
In Commercial Distribution
- 00845533001779 ()
SM9Z7701M
- Parvovirus B19 immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
The ZEUS ELISA Parvovirus B19 IgM Test System is intended for the qualitative detection of IgM class antibodies to human parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human parvovirus B19. The test is also for all symptomatic patients as an aid in the diagnosis of fifth disease (erythema infectiosum). This test is intended for in vitro diagnostic use only.
ZEUS SCIENTIFIC, INC.
9Z7701MB
In Commercial Distribution
- 00845533001762 ()
9Z7701MB
- Parvovirus B19 immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
The ZEUS ELISA Parvovirus B19 IgM Test System is intended for the qualitative detection of IgM class antibodies to human parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human parvovirus B19. The test is also for all symptomatic patients as an aid in the diagnosis of fifth disease (erythema infectiosum). This test is intended for in vitro diagnostic use only.
ZEUS SCIENTIFIC, INC.
9Z7701M
In Commercial Distribution
- 00845533001755 ()
9Z7701M
- Parvovirus B19 immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
The ZEUS ELISA Rubella IgM Test System is designed for the qualitative detection of IgM antibodies to the rubella virus in human serum. The assay is intended to be used to evaluate serologic evidence of active or recent infection with rubella virus, and is for In Vitro diagnostic use.
ZEUS SCIENTIFIC, INC.
SM9Z9801M
In Commercial Distribution
- 00845533001045 ()
SM9Z9801M
- Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
The ZEUS ELISA Rubella IgM Test System is designed for the qualitative detection of IgM antibodies to the rubella virus in human serum. The assay is intended to be used to evaluate serologic evidence of active or recent infection with rubella virus, and is for In Vitro diagnostic use.
ZEUS SCIENTIFIC, INC.
9Z9801M
In Commercial Distribution
- 00845533001038 ()
9Z9801M
- Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
Alinity i HAVAb IgM Controls
Abbott GmbH
08P2810
In Commercial Distribution
- 00380740131579 ()
08P2810
- Hepatitis A virus immunoglobulin M (IgM) antibody IVD, control
ARCHITECT HAVAB-M Controls
Abbott GmbH
6L21-10
In Commercial Distribution
- 00380740011086 ()
06L2110
- Hepatitis A virus immunoglobulin M (IgM) antibody IVD, control
Immunoglobulin M Flex® reagent cartridge, 120 tests
Siemens Healthcare Diagnostics Inc.
10444984
In Commercial Distribution
- 00842768005732 ()
- 00630414004600 ()
DF81
- Immunoglobulin M subclass (IgM subclass) IVD, kit, nephelometry/turbidimetry
The DPP Zika IgM System is intended for the presumptive qualitative detection of Zika virus IgM antibodies in human serum (plain or separation gel), potassium-EDTA plasma, potassium EDTA venous whole blood, or fingerstick whole blood specimens, collected from individuals meeting the CDC Zika virus clinical criteria (e.g., a history of clinical signs and symptoms associated with Zika virus infection) and/or CDC Zika virus epidemiological criteria (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated).
Chembio Diagnostic Systems Inc.
65-9560-0
In Commercial Distribution
- 00607158000106 ()
- Zika virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)