Identity
- Trade Name
- Schistosoma IgG ELISA FDA UDI
- Generic Name
- Schistosoma mansoni immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- For the qualitative determination of serum or plasma antibodies in humans, primarily IgG, to Schistosoma spp. using the ELISA technique. FDA UDI
- Model / Reference
- EIA-3512 FDA UDI
- Description
- For the qualitative determination of serum or plasma antibodies in humans, primarily IgG, to Schistosoma spp. using the ELISA technique. FDA UDI
Identifiers
- Catalog Number
- EIA-3512 FDA UDI
- Primary DI / UDI-DI
- 00840239035127 FDA UDI
- FDA Product Code
- GNH FDA UDI
- GMDN Term
- Schistosoma mansoni immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3600 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: Schistosoma mansoni immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Schistosoma IgG ELISA by DRG International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Schistosoma mansoni immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).
- Schistosoma mansoni IgG ELISA — DRG Instruments Gesellschaft mit beschränkter Haftung · Class I
- Schistosoma IgG ELISA — DRG Instruments Gesellschaft mit beschränkter Haftung · Class I
- Anti-Schistosoma ELISA (IgG) — EUROIMMUN Medizinische Labordiagnostika AG · Class I
- NovaLisa Schistosoma mansoni IgG — Gold Standard Diagnostics Frankfurt GmbH · Class I
- Schistosoma mansoni 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 68360723-c176-411d-9765-b735beaa9ce2 36 fields · synced May 30, 2026