LIAISON QUANTIferon TB Gold Plus

GUDID 08056771602945

USA manufactured kit

Diasorin Inc.

Pregnenolone IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 08056771602945
• NIH Device Record Key: 75ed3b24-1292-41f5-b960-44f71d577242
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON QUANTIferon TB Gold Plus
• Version Model Number: 311020
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056771602945 [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: 2023-09-18
• Device Publish Date: 2023-09-08

Devices Manufactured by Diasorin Inc.

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