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(37898 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ARCHITECT CORE-M Calibrators
Abbott GmbH
6L23-01
In Commercial Distribution

  • 00380740011130 ()
06L2301

  • Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, calibrator
Alinity i Anti-HBc IgM Calibrators
Abbott GmbH
07P8602
In Commercial Distribution

  • 00380740146177 ()
07P8602

  • Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, calibrator
Alinity i Anti-HBc IgM Reagent Kit 200 Tests
Abbott GmbH
07P8621
In Commercial Distribution

  • 00380740130282 ()
07P8621

  • Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay
Alinity i Toxo IgM Calibrator
Abbott GmbH
07P4704
In Commercial Distribution

  • 00380740200626 ()
07P4704

  • Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, calibrator
The ZEUS ELISA Toxoplasma gondii IgM Test System is an enzyme-linked immunosorbent assay designed for the presumptive qualitative detection of IgM antibodies to Toxoplasmaplasma gondii in human serum and for the presumptive diagnosis of acute, recent, or reactive Toxoplasma gondii infection. To adequately assess the patient’s serological status, testing must be performed in conjunction with an anti-Toxoplasma gondii IgG antibody assay. This product is not FDA cleared (approved) for use in screening blood or plasma donors. This assay’s performance has not been established for screening of prenatal women or newborns.
ZEUS SCIENTIFIC, INC.
SM8Z8651M
In Commercial Distribution

  • 00845533001236 ()
SM8Z8651M

  • Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
The ZEUS ELISA Toxoplasma gondii IgM Test System is an enzyme-linked immunosorbent assay designed for the presumptive qualitative detection of IgM antibodies to Toxoplasmaplasma gondii in human serum and for the presumptive diagnosis of acute, recent, or reactive Toxoplasma gondii infection. To adequately assess the patient’s serological status, testing must be performed in conjunction with an anti-Toxoplasma gondii IgG antibody assay. This product is not FDA cleared (approved) for use in screening blood or plasma donors. This assay’s performance has not been established for screening of prenatal women or newborns.
ZEUS SCIENTIFIC, INC.
8Z8651M
In Commercial Distribution

  • 00845533001229 ()
8Z8651M

  • Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
No Description
Roche Diagnostics GmbH
11820567160
Not in Commercial Distribution

  • 04015630911615 ()
11820567160

  • Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay
BioPlex 2200 Lyme Total Control CD
BIO-RAD LABORATORIES, INC.
12000880
In Commercial Distribution

  • 03610520506431 ()

  • 1 Each
12000880

  • Borrelia burgdorferi immunoglobulin G (IgG)/IgM antibody IVD, control
BioPlex 2200 Lyme Total Control Set
BIO-RAD LABORATORIES, INC.
12000879
In Commercial Distribution

  • 03610520506424 ()

  • Total Volume: 1.5 Milliliter
  • 6 Vials
12000879

  • Borrelia burgdorferi immunoglobulin G (IgG)/IgM antibody IVD, control
PLATELIA Toxo IgM
BIO-RAD
26211
In Commercial Distribution

  • 03610520007853 ()
26211

  • Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
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