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(41110 results)
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ACCURUN 113 Hepatitis B Core IgM 1 x 5.0 mL
Lgc Clinical Diagnostics, Inc.
2015-0068
In Commercial Distribution
- 00816784020277 ()
2015-0068
- Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, control
IgM (Immunoglobulin M) 2 x 60 tests
CAROLINA LIQUID CHEMISTRIES CORPORATION
CC638
Not in Commercial Distribution
- 00817302020953 ()
- Total Volume: 8 Milliliter
- Kit contains 2 Reagent cartridges, 1 user defined paramenter and 1 package insert
- Total Volume: 23 Milliliter
CC638
- Hepatitis G virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
"720-630 EBNA-1 IgM Test Kit"
DIAMEDIX CORPORATION
720-630
In Commercial Distribution
- 00817273020341 ()
- Candida albicans immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
"720-610 EBV-VCA IgM Test Kit"
DIAMEDIX CORPORATION
720-610
In Commercial Distribution
- 00817273020327 ()
- Candida albicans immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
"300-312A Toxoplasma IgM Capture Lyoph. Ag. Accessory Kit"
DIAMEDIX CORPORATION
300-312A
In Commercial Distribution
- 00817273020020 ()
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
Detection of Rubella Virus Antibodies
ARLINGTON SCIENTIFIC, INC.
NC-605001
In Commercial Distribution
- 00816057021635 ()
- Total Volume: 1 Milliliter
NC-605001
- Rubella virus immunoglobulin G (IgG)/IgM antibody IVD, control
No Description
Roche Diagnostics GmbH
11876333160
11876333160
- Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, control
Pointe Scientific, Inc. Toxoplasma IgM Reagent is for the qualitative and quantitative detection of human IgM antibodies to Toxoplasma in human serum by enzyme immunoassay, to aid in the diagnosis of Toxoplasma infection. A positive result is presumptive for the detection of anti-Toxoplasma gondii antibodies and presumptive for the diagnosis of acute, recent, or reactivated Toxoplasma gondii infection. Patient testing with anti-Toxoplasma gondii IgM antibody assay, must be accompanied by an anti-Toxoplasma gondii IgG antibody assay. The assay’s performance characteristics have not been established for neonatal toxoplasmosis diagnosis. This assay has not been cleared / approved by the FDA for blood / plasma donor screening. 96 tests.
POINTE SCIENTIFIC, INC.
T8002-96
In Commercial Distribution
- 00811727015167 ()
T8002-96
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
The ImmunoFA Toxo IgM Test is an immunofluorescence test for the presumptive detection and titration of IgM antibodies to Toxoplasma gondii in human serum and is presumptive for the diagnosis of acute, recent, or reactivated T. gondii infection. It is intended that the ImmunoFA Toxo IgG Test be performed in conjunction with this assay. This product is not FDA cleared (approved) for use in testing (i.e., screening) blood or plasma donors.
Genbio
800-1300
Not in Commercial Distribution
- 00613745013008 ()
- 100 tests
1300
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
IgG-coated red blood cells used to confirm negative results in direct antiglobulin test (DAT) and indirect antiglobulin test (IAT).
AMERICAN NATIONAL RED CROSS
510400/510402
In Commercial Distribution
- 20858400005095 ()
- 00858400005091 ()
- 10858400005098 ()
- Immunoglobulin-sensitized reagent red blood cell IVD, control