LIAISON® N-TACT® PTH Gen II Calibration Verifiers

GUDID 08056771600460

Diasorin Inc.

Parathyroid hormone (PTH) IVD, reagent

• Primary Device ID: 08056771600460
• NIH Device Record Key: a1085178-57ca-477e-90b1-01fa1905c16b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIAISON® N-TACT® PTH Gen II Calibration Verifiers
• Version Model Number: 317913
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056771600460 [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: 3
• Public Version Date: 2019-12-23
• Device Publish Date: 2016-09-24

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