Walgreens

GUDID 00311917060897

Walgreens Covid+Flu A&B Antigen Test 2S

WALGREEN CO.

Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing

• Primary Device ID: 00311917060897
• NIH Device Record Key: d5d36822-f6d7-42fe-b448-4aeb2e2290a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Walgreens
• Version Model Number: 172723
• Company DUNS: 008965063
• Company Name: WALGREEN CO.
• 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: false
• Device Combination Product: false
• Single Use: true
• 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: true

Customer Support Contacts

• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-925-4733
• Email: consumerrelations.pq@walgreens.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00311917060897 [Primary]
GS1	10311917060894 [Package]; Package: Case [32 Units]; In Commercial Distribution

FDA Product Code

• SCA: Multi-Analyte Respiratory Virus Antigen Detection Test

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: 2025-01-22
• Device Publish Date: 2025-01-14

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