Identity
- Trade Name
- RealTime FDA UDI
- Generic Name
- Hepatitis C virus genotyping IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- Abbott RealTime HCV Genotype II Amplification Reagent Kit FDA UDI
- Model / Reference
- 08L21-90 FDA UDI
- Description
- Abbott RealTime HCV Genotype II Amplification Reagent Kit FDA UDI
Identifiers
- Catalog Number
- 08L21-90 FDA UDI
- Primary DI / UDI-DI
- 00884999036130 FDA UDI
- PMA Number
- P120012 FDA UDI
- FDA Product Code
- OBF FDA UDI
- GMDN Term
- Hepatitis C virus genotyping IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3170 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
Yes
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 C virus genotyping IVD, kit, nucleic acid technique (NAT)
RealTime by Abbott Molecular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
P120012 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 II | Pending data |
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Manufacturer
- Manufacturer
- Abbott Molecular
Sources (1)
- FDA UDI e616a641-ceff-4728-82aa-01bf86af6e2c 37 fields · synced May 30, 2026