Identity
- Trade Name
- Trinity Biotech FDA UDI
- Generic Name
- Multiple Leishmania species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Leismaniasis IFA Test System, 48 Tests FDA UDI
- Model / Reference
- 20-04648 FDA UDI
- Description
- Leismaniasis IFA Test System, 48 Tests FDA UDI
Identifiers
- Catalog Number
- 20-04648 FDA UDI
- Primary DI / UDI-DI
- 05391516748698 FDA UDI
- FDA Product Code
- LOO FDA UDI
- GMDN Term
- Multiple Leishmania species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3870 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
No
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: Multiple Leishmania species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay
Trinity Biotech by Mardx Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multiple Leishmania species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay.
- Trinity Biotech — MARDX DIAGNOSTICS, 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
- Mardx Diagnostics, Inc.
Sources (1)
- FDA UDI a25ebe51-82cc-4517-a201-0dbe182981ac 36 fields · synced May 31, 2026