Well at Walgreens 170265

GUDID 10049022632834

Plastic Applicator Tampon, Super absorbency 36

WALGREEN CO.

Menstrual tampon, unscented

• Primary Device ID: 10049022632834
• NIH Device Record Key: d5ed58b7-9f28-4944-88d1-b2598d7cf928
• Commercial Distribution Discontinuation: 2016-11-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Well at Walgreens
• Version Model Number: 411505
• Catalog Number: 170265
• Company DUNS: 008965063
• Company Name: WALGREEN CO.
• Device Count: 36
• 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: false
• 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: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com
• Phone: 1-800-228-3273
• Email: consumerrelations.pq@walgreens.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00049022632837 [Primary]
GS1	07290016625059 [Unit of Use]
GS1	10049022632834 [Package]; Contains: 00049022632837; Package: Case [6 Units]; Discontinued: 2016-11-21; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020535

FDA Product Code

• HEB: Tampon, Menstrual, Unscented

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-12-09
• Device Publish Date: 2016-11-16

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