3M™ Clinpro™ 7220SP

GUDID 50605861084029

3M™ Clinpro™ Clear Fluoride Treatment, 7220SP, Sample Pack, 0.5 mL Unit Dose, 3/KT

3M COMPANY

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• Primary Device ID: 50605861084029
• NIH Device Record Key: b9fdc45b-b93d-49d7-947e-09decc2080a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Clinpro™
• Version Model Number: 7220SP
• Catalog Number: 7220SP
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• 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: true
• 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(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10605861084021 [Primary]
GS1	50605861084029 [Package]; Contains: 10605861084021; Package: BOX [54 Units]; In Commercial Distribution

FDA Product Code

• LBH: VARNISH, CAVITY

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: 2023-12-22
• Device Publish Date: 2023-12-14

On-Brand Devices [3M™ Clinpro™]

• 50605861084029: 3M™ Clinpro™ Clear Fluoride Treatment, 7220SP, Sample Pack, 0.5 mL Unit Dose, 3/KT
• 50605861084012: 3M™ Clinpro™ Clear Fluoride Treatment, 7210FF, Flavorless, 0.5 mL Unit Dose, 100/PAC
• 50605861084005: 3M™ Clinpro™ Clear Fluoride Treatment, 7210W, Watermelon Flavor, 0.5 mL Unit Dose, 100/PAC
• 50605861083992: 3M™ Clinpro™ Clear Fluoride Treatment, 7210M, Mint Flavor, 0.5 mL Unit Dose, 100/PAC
• 50605861083985: 3M™ Clinpro™ Clear Fluoride Treatment, 7200FF, Flavorless, 0.5 mL Unit Dose, 50/PAC
• 50605861083978: 3M™ Clinpro™ Clear Fluoride Treatment, 7200W, Watermelon Flavor, 0.5 mL Unit Dose, 50/PAC
• 50605861083961: 3M™ Clinpro™ Clear Fluoride Treatment, 7200M, Mint Flavor, 0.5 mL Unit Dose, 50/PAC