Identity
- Trade Name
- T-SPOT®.TB50 FDA UDI
- Generic Name
- Mycobacterium tuberculosis complex species antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- For the detection of effector t cells that respond to stimulation by mycobacterium tuberculosis antigens esat-6 and cfp-10 and indicated for use as an aid in the diagnosis of M.Tuberculosis infection in conjunction with risk assessment, radiography and other medical diagnostic evaluations. FDA UDI
- Model / Reference
- TB.50 FDA UDI
- Description
- For the detection of effector t cells that respond to stimulation by mycobacterium tuberculosis antigens esat-6 and cfp-10 and indicated for use as an aid in the diagnosis of M.Tuberculosis infection in conjunction with risk assessment, radiography and other medical diagnostic evaluations. FDA UDI
Identifiers
- Catalog Number
- TB.50US FDA UDI
- Primary DI / UDI-DI
- 15051716000046 FDA UDI
- PMA Number
- P070006 FDA UDI
- FDA Product Code
- OJN FDA UDI
- GMDN Term
- Mycobacterium tuberculosis complex species antigen IVD, kit, enzyme immunoassay (EIA) 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
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: Mycobacterium tuberculosis complex species antigen IVD, kit, enzyme immunoassay (EIA)
T-Spot®.tb50 by Oxford Immunotec, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mycobacterium tuberculosis complex species antigen IVD, kit, enzyme immunoassay (EIA).
- T-SPOT®.TB8 — Oxford Immunotec, Inc. · Class III
- T-SPOT®.TB96 — Oxford Immunotec, Inc. · Class III
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 III | Pending data |
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Manufacturer
- Manufacturer
- Oxford Immunotec, Inc.
Sources (1)
- FDA UDI e41cab65-8c23-40c3-bedd-7709d33cbef5 36 fields · synced May 30, 2026