LIAISON QUANTIferon TB Gold Plus

GUDID 08056771603300

DIASORIN SPA

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• Primary Device ID: 08056771603300
• NIH Device Record Key: 3f13d977-4390-4ec9-9b7a-96382d9e5038
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON QUANTIferon TB Gold Plus
• Version Model Number: 311040
• Company DUNS: 630822989
• Company Name: DIASORIN SPA
• 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	08056771603300 [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: 2023-07-31
• Device Publish Date: 2023-07-21

On-Brand Devices [LIAISON QUANTIferon TB Gold Plus]

• 08056771103268: 311020
• 08056771603300: 311040
• 08056771104081: Italy manufactured kit.
• 08056771104098: Italy manufactured kit.