Identity
- Trade Name
- MONOLISA™ FDA UDI
- Generic Name
- Hepatitis B virus core antigen IVD, reagent FDA UDI
- Device Name
- Anti-HBc EIA, Conjugate Reagent 30 mL FDA UDI
- Model / Reference
- 26193 FDA UDI
- Description
- Anti-HBc EIA, Conjugate Reagent 30 mL FDA UDI
Identifiers
- Catalog Number
- 26193 FDA UDI
- Primary DI / UDI-DI
- 00847865013079 FDA UDI
- PMA Number
- P060031 FDA UDI
- FDA Product Code
- LOM FDA UDI
- GMDN Term
- Hepatitis B virus core antigen IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3172 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 30 Milliliter FDA UDI
Category: Hepatitis B virus core antigen IVD, reagent
Monolisa™ by Bio-Rad Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hepatitis B virus core antigen IVD, reagent.
- MONOLISA™ — Bio-Rad Laboratories · Class II
Cleared under the same submission
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio-Rad Laboratories
Sources (1)
- FDA UDI 6315a596-24f5-4f4c-9022-944652beb3bc 38 fields · synced Jun 1, 2026