3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 6697CA

GUDID 50707387815566

3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 2 Incise Film and Clear Screen, 6697CA, 5/CS

3M COMPANY

Patient surgical drape, single-use

• Primary Device ID: 50707387815566
• NIH Device Record Key: e3f6fae9-0121-43d4-a376-b1a4fd75cf21
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™
• Version Model Number: 6697CA
• Catalog Number: 6697CA
• 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: true
• 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: 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	10707387815568 [Primary]
GS1	50707387815566 [Package]; Contains: 10707387815568; Package: CV [5 Units]; In Commercial Distribution

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: 2024-09-23
• Device Publish Date: 2024-09-13

Devices Manufactured by 3M COMPANY

• 50707387815566 - 3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™: 2024-09-233M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 2 Incise Film and Clear Screen, 6697CA, 5/CS
• 50707387815566 - 3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™: 2024-09-23 3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 2 Incise Film and Clear Screen, 6697CA, 5/CS
• 50707387814583 - 3M™: 2024-08-27 3M™ Surgical Clipper with Pivoting Head, 9661L, 1 Each/Case
• 50707387814590 - 3M™: 2024-08-27 3M™ Surgical Clipper with Pivoting Head, 9667L, 1/Case
• 50707387814606 - 3M™: 2024-08-27 3M™ Surgical Clipper Starter Kit (9661L Clipper and 9663L Charger Stand) 9667L-A
• 50707387814613 - 3M™: 2024-08-27 3M™ Surgical Clipper Starter Kit (9661L Clipper and 9668L Charger Stand) 9667L-E
• 00707387000011 - Red Dot™: 2024-08-23 3M™ Red Dot™ Trace Prep 2236
• 00707387815042 - 3M Company: 2024-08-23 2954 MEDIPORE PRE-CUT DSG CVR 10CMX12CM
• 00707387815059 - 3M Company: 2024-08-23 2955 MEDIPORE PRE-CUT DSG CVR 10CMX20CM