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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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Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA - 00840239051899

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 International Inc
EIA-5189
In Commercial Distribution

  • 00840239051899 ()
EIA-5189

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

Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA - 00840239051882

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 International Inc
EIA-5188
In Commercial Distribution

  • 00840239051882 ()
EIA-5188

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

CHORUS Q FEVER PHASE II IgG - 08033891322083

No Description
DIESSE DIAGNOSTICA SENESE SPA
81171
In Commercial Distribution

  • 08033891322083 ()
81171

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

Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA - 04048474051896

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)

Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA - 04048474051889

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)

NovaLisa Coxiella burnetii (Q-Fever) Phase 2 IgG - ENTICOX2G0600

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).
Gold Standard Diagnostics Frankfurt GmbH
COX2G060
In Commercial Distribution

  • ENTICOX2G0600 ()
COX2G0600

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

NovaLisa Coxiella burnetii (Q-Fever) Phase 1 IgG - ENTICOX1G0600

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).
Gold Standard Diagnostics Frankfurt GmbH
COX1G060
In Commercial Distribution

  • ENTICOX1G0600 ()
COX1G0600

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

C. burnetii 12 Well 10 pk - 00813545026073

No Description
SCIMEDX CORPORATION
I-QFB01X
In Commercial Distribution

  • 00813545026073 ()
I-QFB01X

  • Coxiella burnetii total antibody IVD, kit, fluorescent immunoassay

JBAIDS - 00851458005013

JBAIDS IVD Q Fever Detection Kit
BIOFIRE DEFENSE, LLC
JRPD-ASY-0016
Not in Commercial Distribution

  • 00851458005013 ()
JRPD-ASY-0016

  • Coxiella burnetii nucleic acid IVD, kit, nucleic acid technique (NAT)

N/A - 00681490902939

INSTRUMENT 8691016 CRSLK MSR TL CRD 19MM
MEDTRONIC SOFAMOR DANEK, INC.
8691016
In Commercial Distribution

  • 00681490902939 ()


  • Bone-screw internal spinal fixation system connector
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