Identity
- Trade Name
- LIAISON QUANTIferon TB Gold Plus FDA UDI
- Generic Name
- Interferon IVD, kit, chemiluminescent immunoassay FDA UDI
- Device Name
- US manufactured kit FDA UDI
- Model / Reference
- 311040 FDA UDI
- Description
- US manufactured kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08056771603300 FDA UDI
- FDA Product Code
- NCD FDA UDI
- GMDN Term
- Interferon IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Category: Interferon IVD, kit, chemiluminescent immunoassay
LIAISON QUANTIferon TB Gold Plus by Diasorin Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Interferon IVD, kit, chemiluminescent immunoassay.
- LIAISON QUANTIferon TB Gold Plus — Diasorin Inc. · Class III
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Diasorin Inc.
Sources (1)
- FDA UDI 3f13d977-4390-4ec9-9b7a-96382d9e5038 33 fields · synced May 30, 2026