ComforTENS Plus MU73490

GUDID 90884521170304

True content to be populated as part of rebranding

Cardinal Health, Inc.

Transcutaneous electrical stimulation lead

• Primary Device ID: 90884521170304
• NIH Device Record Key: ede597dc-ca4b-4737-9e14-ec3b44c82847
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ComforTENS Plus
• Version Model Number: MU73490
• Catalog Number: MU73490
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• Device Count: 48
• 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: false
• Single Use: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521535978 [Unit of Use]
GS1	90884521170304 [Primary]

FDA Product Code

• GXY: ELECTRODE, CUTANEOUS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-02-15
• Device Publish Date: 2016-09-24

On-Brand Devices [ComforTENS Plus]

• 90884521170304: True content to be populated as part of rebranding
• 90884521162910: True content to be populated as part of rebranding
• 10884521170308: True content to be populated as part of rebranding
• 10884521162914: True content to be populated as part of rebranding
• 20884521706269: TENS, Analog