Red Dot™ 2236

GUDID 00707387000011

3M™ Red Dot™ Trace Prep 2236

3M COMPANY

Electrode skin abrasion pad

• Primary Device ID: 00707387000011
• NIH Device Record Key: 9e269e4a-7c32-40af-81e9-564879978155
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Red Dot™
• Version Model Number: 2236
• Catalog Number: 2236
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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	00707387000011 [Primary]

FDA Product Code

• DRX: Electrode, electrocardiograph

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: 2024-08-23
• Device Publish Date: 2024-08-15

On-Brand Devices [Red Dot™]

• 50707387472820: 3M™ Red Dot™ Resting EKG Electrode 2360
• 50707387569278: 3M™ Red Dot™ Neonatal ECG Radiolucent Monitoring Electrode, Pre-Wired, 3 per Bag, 100 Bags p
• 50707387496024: 2280 RD NEONATE ECG MON ELC MET PREWIRED 3/PCH 100 PCH/CASE
• 50707387468571: 3M™ Red Dot™ Neonatal Limb Band Monitoring Electrode, Pre-Wired 2284
• 50707387468564: 3M™ Red Dot™ Infant, Pre-Wired, Radiolucent Monitoring Electrode 2283
• 50707387468557: 3M™ Red Dot™ Neonatal, Pre-Wired, Radiolucent Monitoring Electrode with Soft Cloth 2282
• 50707387000016: 3M™ Red Dot™ Trace Prep 2236
• 50707387212693: 3M™ Red Dot™ Resting EKG Electrode, Amerinet Choice, 10 per Carton, 4 Cartons / Case, 9650
• 00707387000011: 3M™ Red Dot™ Trace Prep 2236