3M™ Unitek™ Clarity™ 003-301

GUDID 00652221287229

Clarity Ultra SL Bkt MBT U Lt Central 17T/4A 022

3M UNITEK CORPORATION

Orthodontic bracket, ceramic

• Primary Device ID: 00652221287229
• NIH Device Record Key: 9e88eb76-7342-4413-8f4d-936f9d54164c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Unitek™ Clarity™
• Version Model Number: 003-301
• Catalog Number: 003-301
• Company DUNS: 008256356
• Company Name: 3M UNITEK CORPORATION
• Device Count: 5
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)423-4588
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)423-4588
• Email: 3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00652221287229 [Primary]
GS1	80652221287225 [Unit of Use]

FDA Product Code

• NJM: Bracket, ceramic, orthodontic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-02-12
• Device Publish Date: 2018-10-23

On-Brand Devices [3M™ Unitek™ Clarity™]

• 00652221287458: Clarity Ultra SL Bkt MBT U Lt/Rt 5X5 Hk 022
• 00652221287434: Clarity Ultra SL Bkt MBT U/L Lt/Rt 5X5 Hk 022
• 00652221287229: Clarity Ultra SL Bkt MBT U Lt Central 17T/4A 022