Identity
- Trade Name
- Sofia FDA UDI
- Generic Name
- Fluorescent immunoassay analyser IVD, point-of-care FDA UDI
- Device Name
- Sofia Analyzer FDA UDI
- Model / Reference
- 20299 FDA UDI
- Description
- Sofia Analyzer FDA UDI
Identifiers
- Catalog Number
- 20299 FDA UDI
- Primary DI / UDI-DI
- 30014613336341 FDA UDI
- 510(k) Number
- K162911 FDA UDI
- FDA Product Code
- KHO FDA UDI
- GMDN Term
- Fluorescent immunoassay analyser IVD, point-of-care FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2560 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Fluorescent immunoassay analyser IVD, point-of-care
Sofia by Quidel Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Sofia — Quidel Corp. · Class I
- Sofia — Quidel Corp. · Class I
- Sofia — Quidel Corp. · Class I
Cleared under the same submission
K162911 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
- Quidel Corp.
Sources (1)
- FDA UDI e3ff4f23-2613-490d-8967-92d0590f637b 36 fields · synced May 29, 2026