ANAFAST™ ANA Fluorescent Test System 240 Wells

GUDID 08056771600859

Diasorin Inc.

Multiple antinuclear antibody (ANA) IVD, kit, fluorescent immunoassay

• Primary Device ID: 08056771600859
• NIH Device Record Key: 2918f05a-e426-4e4b-b476-0d6edfd0b9f3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ANAFAST™ ANA Fluorescent Test System 240 Wells
• Version Model Number: 1670
• 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
• 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
• 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	08056771600859 [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: 2026-02-09
• Device Publish Date: 2016-09-24

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• 08056771600859 - ANAFAST™ ANA Fluorescent Test System 240 Wells: 2026-02-09