Red Dot™ 2360

GUDID 50707387472820

3M™ Red Dot™ Resting EKG Electrode 2360

3M COMPANY

Electrocardiographic electrode, single-use Electrocardiographic electrode, single-use

• Primary Device ID: 50707387472820
• NIH Device Record Key: 3405aa21-42aa-4477-9ef5-c545b36a37da
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Red Dot™
• Version Model Number: 2360
• Catalog Number: 2360
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00707387472825 [Primary]
GS1	10707387472822 [Unit of Use]
GS1	50707387472820 [Package]; Contains: 00707387472825; Package: BOX [40 Units]; In Commercial Distribution

FDA Product Code

• DRX: Electrode, electrocardiograph

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: 2018-03-29
• Device Publish Date: 2016-09-24

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