Identity
- Trade Name
- Toxocara IgG ELISA FDA UDI
- Generic Name
- Toxocara canis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- The Toxocara ELISA test is a semi-quantitative enzyme immunoassay for the detection of antibodies to Toxocara, in samples of human serum or plasma. FDA UDI
- Model / Reference
- EIA-3518 FDA UDI
- Description
- The Toxocara ELISA test is a semi-quantitative enzyme immunoassay for the detection of antibodies to Toxocara, in samples of human serum or plasma. FDA UDI
Identifiers
- Catalog Number
- EIA-3518 FDA UDI
- Primary DI / UDI-DI
- 00840239035189 FDA UDI
- FDA Product Code
- GMO FDA UDI
- GMDN Term
- Toxocara canis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3220 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
No
FDA UDI
Category: Toxocara canis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Toxocara IgG ELISA by DRG International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Toxocara canis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).
- AccuDiag ™ — Diagnostic Automation, Inc. · Class II
- Toxocara canis IgG ELISA Test Kit — Gold Standard Diagnostics, LLC · Class I
- NovaLisa Toxocara canis IgG — Gold Standard Diagnostics Frankfurt GmbH · Class I
- Toxocara IgG ELISA — DRG Instruments Gesellschaft mit beschränkter Haftung · Class II
- Anti-Toxocara ELISA (IgG) — EUROIMMUN Medizinische Labordiagnostika AG · Class I
- Toxocara Antibody 96 Tests — Scimedx Corp. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- DRG International, Inc.
Sources (1)
- FDA UDI d21d957e-602a-499d-bfbb-be9574bc4219 36 fields · synced May 30, 2026