Identity
- Trade Name
- MONOLISA FDA UDI
- Generic Name
- Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- MONOLISA Anti-HAV EIA FDA UDI
- Model / Reference
- 72496 FDA UDI
- Description
- MONOLISA Anti-HAV EIA FDA UDI
Identifiers
- Catalog Number
- 72496 FDA UDI
- Primary DI / UDI-DI
- 00847865012362 FDA UDI
- 510(k) Number
- K092355 FDA UDI
- FDA Product Code
- LOL FDA UDI
- GMDN Term
- Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3310 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
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: Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA)
Monolisa by Bio-Rad — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA).
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
- Bio-Rad
Sources (1)
- FDA UDI 1ea960e5-1545-49e2-aac5-7f697f4b8892 37 fields · synced May 30, 2026