LIAISON® Calprotectin Calibration Verifiers

GUDID 08056771602037

Diasorin Inc.

Calprotectin IVD, calibrator

• Primary Device ID: 08056771602037
• NIH Device Record Key: dbcc3f43-bfa7-4324-a791-76430c8916da
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON® Calprotectin Calibration Verifiers
• Version Model Number: 318963
• 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: 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

Customer Support Contacts

• Phone: 651-439-9710
• Email: info@diasorin.com
• Phone: 651-439-9710
• Email: info@diasorin.com
• Phone: 651-439-9710
• Email: info@diasorin.com
• Phone: 651-439-9710
• Email: info@diasorin.com
• Phone: 651-439-9710
• Email: info@diasorin.com
• Phone: 651-439-9710
• Email: info@diasorin.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056771602037 [Primary]

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-06-10
• Device Publish Date: 2019-02-19

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