Identity
- Trade Name
- Trinity Biotech FDA UDI
- Generic Name
- Measles virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- Captia™ Measles IgG FDA UDI
- Model / Reference
- 2326001 FDA UDI
- Description
- Captia™ Measles IgG FDA UDI
Identifiers
- Catalog Number
- 2326001 FDA UDI
- Primary DI / UDI-DI
- 05391516747127 FDA UDI
- 510(k) Number
- K873925 FDA UDI
- FDA Product Code
- LJB FDA UDI
- GMDN Term
- Measles virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3520 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Measles virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Trinity Biotech by Clark Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Measles virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).
- Gold Standard Diagnostics Is-Measles IgG ELISA Test Kit — Gold Standard Diagnostics, LLC · Class I
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- ReQuest — QUEST INTERNATIONAL, INC. · Class I
- VIDAS® Measles IgG — BIOMERIEUX , INC. · Class I
- QMedix™ — Diagnostic Automation, Inc. · Class I
- NovaLisa Measles Virus IgG — Gold Standard Diagnostics Frankfurt GmbH · Class I
- ELISA Measles IgG Smart Kit Test System — ZEUS SCIENTIFIC, INC.
Cleared under the same submission
K873925 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Clark Laboratories, Inc.
Sources (1)
- FDA UDI 8e921624-4474-4852-aef9-5c4ad8fcfd0b 38 fields · synced May 30, 2026