Sofia 20218

GUDID 30014613202189

Sofia Flu A+B 25T

QUIDEL CORPORATION

Influenza A/B virus antigen IVD, kit, immunochromatographic test (ICT), rapid Influenza A/B virus antigen IVD, kit, immunochromatographic test (ICT), rapid Influenza A/B virus antigen IVD, kit, rapid ICT, clinical Influenza A/B virus antigen IVD, kit, rapid ICT, clinical Influenza A/B virus antigen IVD, kit, rapid ICT, clinical Influenza A/B virus antigen IVD, kit, rapid ICT, clinical Influenza A/B virus antigen IVD, kit, rapid ICT, clinical Influenza A/B virus antigen IVD, kit, rapid ICT, clinical Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay Influenza A virus antigen IVD, kit, fluorescent immunoassay

• Primary Device ID: 30014613202189
• NIH Device Record Key: 3a6881ea-9542-49ce-875e-d35d846a2cee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sofia
• Version Model Number: 20218
• Catalog Number: 20218
• Company DUNS: 079509836
• Company Name: QUIDEL CORPORATION
• 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: true
• Lot Batch: true
• Serial Number: true
• 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: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	30014613202189 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112177

FDA Product Code

• GNX: ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C

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: 2018-12-11
• Device Publish Date: 2018-11-10

On-Brand Devices [Sofia]

• 30014613802211: Sofia Analyzer, Reconditioned
• 30014613202981: Sofia Lyme FIA
• 30014613202769: Sofia Strep A+ 25T
• 30014613202745: Sofia Strep A+ 25T, US
• 30014613202660: Sofia hCG 50T
• 30014613202608: Sofia RSV 25T, US
• 30014613202547: Sofia Flu A+B 25T
• 30014613202530: Sofia Strep A 25T, US
• 30014613202424: Sofia RSV 25T
• 30014613202318: Sofia Strep A 25T
• 30014613202295: Sofia hCG 50T, US
• 30014613202219: Sofia Analyzer
• 30014613202189: Sofia Flu A+B 25T
• 30014613337799: Sofia2 Lyme WB 25T, US
• 30014613336648: Sofia Analyzer
• 30014613336341: Sofia Analyzer
• 30014613339229: Sofia®2 Flu + SARS Antigen FIA
• 30014613339083: Sofia® SARS Antigen FIA