3M™ Steri-Drape™ Cardio/Chest Drape with Ioban™ 6682

GUDID 10707387815629

3M™ Steri-Drape™ Cardio/Chest Drape with Ioban™ 2 Incise Film, 6682, 8/CS

3M COMPANY

Patient surgical drape, single-use

• Primary Device ID: 10707387815629
• NIH Device Record Key: 9ee38ef2-9beb-4e53-9315-93b76ae12891
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Steri-Drape™ Cardio/Chest Drape with Ioban™
• Version Model Number: 6682
• Catalog Number: 6682
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• Device Count: 8
• 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: true
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

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	10707387815629 [Unit of Use]
GS1	50707387815627 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K801550

FDA Product Code

• KKX: Drape, surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-20
• Device Publish Date: 2024-08-12

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• 50707387789904 - 3M™ Littmann® Cardiology IV™: 2024-11-25 3M™ Littmann® Cardiology IV™ Diagnostic Stethoscope, 6171, Smoke-Finish Chestpiece, Turquoise Tube, Smoke Stem