gammaCore Emerald 50022-00004-RPL

GUDID 00815203022717

gammaCore Emerald Charging Cable - Replacement

electroCore, Inc.

Migraine-therapy peripheral nerve electrical stimulator

• Primary Device ID: 00815203022717
• NIH Device Record Key: 4ade4d54-57f8-40f3-9ead-1232c5927444
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: gammaCore Emerald
• Version Model Number: 50022-00004-RPL
• Catalog Number: 50022-00004-RPL
• Company DUNS: 831341628
• Company Name: electroCore, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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: 1-888-903-2673
• Email: customerservice@electrocore.com
• Phone: 1-888-903-2673
• Email: customerservice@electrocore.com
• Phone: 1-888-903-2673
• Email: customerservice@electrocore.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815203022717 [Primary]

FDA Product Code

• QAK: Non-Invasive Vagus Nerve Stimulator For Migraine Headache

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: 2026-02-24
• Device Publish Date: 2026-02-16

On-Brand Devices [gammaCore Emerald]

• 00815203022724: gammaCore Emerald Charging Block - Replacement
• 00815203022717: gammaCore Emerald Charging Cable - Replacement
• 00815203022700: gammaCore Emerald Handset Assembly - Replacement
• 00815203022694: gammaCore Emerald Charging Pad - Replacement