LIAISON XL MUREX HBeAg

GUDID 18056771103401

DIASORIN SPA

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• Primary Device ID: 18056771103401
• NIH Device Record Key: fcadcd63-1929-41a3-9a3e-2be2ecbf7180
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON XL MUREX HBeAg
• Version Model Number: 318150
• 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	08056771103404 [Primary]
GS1	18056771103401 [Package]; Contains: 08056771103404; Package: [10 Units]; In Commercial Distribution

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: 2021-04-21
• Device Publish Date: 2021-04-13

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