Marc Pro, Inc

GUDID 00854784005023

Electrode, Cutaneous

MARC PRO

Transcutaneous electrical stimulation electrode Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 00854784005023
• NIH Device Record Key: 747aa021-21eb-41f3-850e-5347d15e15c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Marc Pro, Inc
• Version Model Number: 70011
• Company DUNS: 042947847
• Company Name: MARC PRO
• 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: false
• Single Use: false
• 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: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com
• Phone: 855-627-2776
• Email: contact@marcpro.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00854784005023 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130987

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-15

On-Brand Devices [Marc Pro, Inc]

• 00854784005023: Electrode, Cutaneous
• 00854784005016: MPP