LIAISON® XL MUREX Anti-HBs Verifiers

GUDID 08056771103466

DIASORIN SPA

Hepatitis B virus surface total antibody IVD, control

• Primary Device ID: 08056771103466
• NIH Device Record Key: 005e93c8-0666-4ac4-b584-9bba39701ede
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON® XL MUREX Anti-HBs Verifiers
• Version Model Number: 318223
• 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: true
• 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	08056771103466 [Primary]

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: 2020-03-06
• Device Publish Date: 2020-02-27

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