LIAISON QuantiFERON TB Gold Plus II

GUDID 08056771104401

US manufactured kit

Diasorin Inc.

Interferon IVD, kit, chemiluminescent immunoassay

• Primary Device ID: 08056771104401
• NIH Device Record Key: c98879e4-6248-4450-8666-ae342ba3bb03
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON QuantiFERON TB Gold Plus II
• Version Model Number: 311080
• Company DUNS: 033429783
• Company Name: Diasorin Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056771104401 [Primary]

FDA Product Code

• NCD: Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-27
• Device Publish Date: 2026-02-19

Devices Manufactured by Diasorin Inc.

• 08056771104401 - LIAISON QuantiFERON TB Gold Plus II: 2026-02-27US manufactured kit
• 08056771104401 - LIAISON QuantiFERON TB Gold Plus II: 2026-02-27 US manufactured kit
• 08056771600811 - ANAFLUOR™: 2026-02-09
• 08056771600828 - ANAFLUOR™: 2026-02-09
• 08056771600835 - ANAFLUOR ™: 2026-02-09
• 08056771600842 - ANAFLUOR™: 2026-02-09
• 08056771600859 - ANAFAST™ ANA Fluorescent Test System 240 Wells: 2026-02-09
• 08056771600897 - CT-3 Immunoscreen Fluoro-Kit™: 2026-02-09
• 08056771600903 - CT-2 Immunoscreen Fluoro-Kit™: 2026-02-09