Identity
- Trade Name
- HIV-1 Antibody Test Controls FDA UDI
- Generic Name
- HIV1 antibody IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- HIV-1 Antibody Test Controls (Test Controls) are external quality control agents intended for use only with Reveal G4. FDA UDI
- Model / Reference
- 815311007590 FDA UDI
- Description
- HIV-1 Antibody Test Controls (Test Controls) are external quality control agents intended for use only with Reveal G4. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00628451188087 FDA UDI
- FDA Product Code
- MZF FDA UDI
- GMDN Term
- HIV1 antibody IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3956 FDA UDI
- Commercial Distribution
- Not 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
HIV-1 Antibody Test Controls by MedMira Laboratories Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- MedMira Laboratories Inc
Sources (1)
- FDA UDI fb58dc18-5648-407f-a6a5-dd6e35cfb848 35 fields · synced Jun 1, 2026