3M™ Steri-Drape™ Craniotomy Pack with Ioban™ 6687P

GUDID 10707387815612

3M™ Steri-Drape™ Craniotomy Pack with Ioban™ 2 Incise Film, 6687P, 7/CS

3M COMPANY

Patient surgical drape, single-use

• Primary Device ID: 10707387815612
• NIH Device Record Key: 1f4a7e31-657c-4927-bbb3-f7948c269e54
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Steri-Drape™ Craniotomy Pack with Ioban™
• Version Model Number: 6687P
• Catalog Number: 6687P
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• Device Count: 7
• 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	10707387815612 [Unit of Use]
GS1	50707387815610 [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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• 50605861085897 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A3, A3, 0.2 g, Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085903 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A3.5, A3.5, 0.2 g, Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085910 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A4, A4, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085927 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550B1, B1, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085934 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550B2, B2, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085941 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550D3, D3, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS