Identity
- Trade Name
- Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA FDA UDI
- Generic Name
- Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- 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). FDA UDI
- Model / Reference
- EIA-5188 FDA UDI
- Description
- 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). FDA UDI
Identifiers
- Catalog Number
- EIA-5188 FDA UDI
- Primary DI / UDI-DI
- 00840239051882 FDA UDI
- FDA Product Code
- GPR FDA UDI
- GMDN Term
- Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA by DRG International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).
- Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA — DRG Instruments Gesellschaft mit beschränkter Haftung · Class I
- Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA — DRG Instruments Gesellschaft mit beschränkter Haftung · Class I
- NovaLisa Coxiella burnetii (Q-Fever) Phase 1 IgG — Gold Standard Diagnostics Frankfurt GmbH · Class I
- NovaLisa Coxiella burnetii (Q-Fever) Phase 2 IgG — Gold Standard Diagnostics Frankfurt GmbH · Class I
- CHORUS Q FEVER PHASE II IgG — DIESSE DIAGNOSTICA SENESE SPA · Class I
- Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA — DRG International, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- DRG International, Inc.
Sources (1)
- FDA UDI 2138df70-9ada-4c5d-bf54-656c3f601acb 36 fields · synced May 30, 2026