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(34858 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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No Description
MONOBIND, INC.
1525-300
In Commercial Distribution

  • 00816870021096 ()

  • Width: 7.75 Inch
1525-300A

  • Helicobacter pylori immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
No Description
MONOBIND, INC.
1475-300
In Commercial Distribution

  • 00816870022741 ()

  • Width: 7.75 Inch
1475-300A

  • Helicobacter pylori immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
No Description
DIASORIN MOLECULAR LLC
EL0300M-5
In Commercial Distribution

  • 20816101022032 ()
EL0300M-5

  • West Nile virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
No Description
DIASORIN MOLECULAR LLC
EL0300M
In Commercial Distribution

  • 20816101022025 ()
EL0300M

  • West Nile virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
Positive control for use with ImmunoFA Toxoplasma IgM kit.
Genbio
800-1341
Not in Commercial Distribution

  • 00613745013411 ()

  • 1.0 mL
1341

  • Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, control
The ZEUS IFA Toxoplasma gondii IgM Test System is an indirect fluorescent antibody assay designed for the presumptive qualitative detection of IgM antibodies to T. gondii in human serum and for the presumptive diagnosis of acute, recent, or reactive T. gondii infection. To adquately assess the patient’s serological status; testing must be performed in conjunction with an anti-T. gondii IgG antibody assay. This product is not FDA cleared (approved) for use in testing (i.e., screening) blood or plasma donors. Performance characteristics have not been established for screening sera from prenatal women or newborns.
ZEUS SCIENTIFIC, INC.
FA8001M
In Commercial Distribution

  • 00845533001526 ()
FA8001M

  • Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
T. pallidum WB IgG Positive Control, 250µl
MARDX DIAGNOSTICS, INC.
40-5023
In Commercial Distribution

  • 05391516749138 ()
40-5023

  • Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control
T. pallidum WB Negative Control, 250µl
MARDX DIAGNOSTICS, INC.
40-5021
In Commercial Distribution

  • 05391516749121 ()
40-5021

  • Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control
PK7400 TP HA CONTROLS is intended for use with the PK7400 TP HA REAGENT (B11186) for the qualitative screening of blood and plasma donors for the detection of Treponema pallidum IgG and IgM antibodies in human serum, EDTA plasma and CPDA plasma using the Beckman Coulter PK7400 Automated Microplate System.
NEWMARKET BIOMEDICAL LIMITED
B11187
In Commercial Distribution

  • 05060515140047 ()

  • 16 x 5mL


  • Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control
Respiratory Panel Cartridge
GENMARK DIAGNOSTICS, INC.
ePlex Respiratory Panel (RP)
In Commercial Distribution

  • 00857167005016 ()
KT022287

  • Hepatitis G virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
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