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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.
11925-300
In Commercial Distribution

  • 00816870023595 ()

  • Width: 7.75 Inch
11925-300A

  • SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
"720-640 EBV-EA-D IgG Test Kit"
DIAMEDIX CORPORATION
720-640
In Commercial Distribution

  • 00817273020358 ()


  • Echinococcus granulosus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
"720-460 anti-TG IgG Test Kit"
DIAMEDIX CORPORATION
720-460
In Commercial Distribution

  • 00817273020273 ()


  • Echinococcus multilocularis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
"720-450 anti-TPO IgG Test Kit"
DIAMEDIX CORPORATION
720-450
In Commercial Distribution

  • 00817273020266 ()


  • Echinococcus multilocularis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
"720-440 anti-PR-3 (C-ANCA) IgG Test Kit"
DIAMEDIX CORPORATION
720-440
In Commercial Distribution

  • 00817273020259 ()


  • Echinococcus multilocularis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
"720-430 anti-MPO (P-ANCA) IgG Test Kit"
DIAMEDIX CORPORATION
720-430
In Commercial Distribution

  • 00817273020242 ()


  • Echinococcus multilocularis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
No Description
Roche Diagnostics GmbH
09203095190
In Commercial Distribution

  • 07613336179451 ()
09203095190

  • SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, chemiluminescent immunoassay
No Description
Roche Diagnostics GmbH
09203079190
In Commercial Distribution

  • 07613336179444 ()
09203079190

  • SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, chemiluminescent immunoassay
The Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA is intended for the qualitative determination of IgG class antibodies against Coxiella burnetii (Q-Fever) Phase 2 in human serum or plasma (citrate, heparin).
DRG Instruments Gesellschaft mit beschränkter Haftung
EIA-5189
In Commercial Distribution

  • 04048474051896 ()
EIA-5189

  • Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
The Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA is intended for the qualitative determination of IgG class antibodies against Coxiella burnetii (Q-Fever) Phase 1 in human serum or plasma (citrate, heparin).
DRG Instruments Gesellschaft mit beschränkter Haftung
EIA-5188
In Commercial Distribution

  • 04048474051889 ()
EIA-5188

  • Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
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