Quell Charger Cable

GUDID 00851221006780

Quell Charger Cable

NeuroMetrix, Inc.

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 00851221006780
• NIH Device Record Key: 78a6a3e4-ba03-4e7b-809a-3b90985c7207
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quell Charger Cable
• Version Model Number: QE-CH2
• Company DUNS: 957536014
• Company Name: NeuroMetrix, 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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: 1-888-903-2673
• Email: customerservice@electrocore.com
• Phone: 1-888-903-2673
• Email: customerservice@electrocore.com
• Phone: 1-888-903-2673
• Email: customerservice@electrocore.com
• 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
• 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
• 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
• 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	00851221006780 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• deNovo: DEN210046

FDA Product Code

• QSQ: Transcutaneous Electrical Nerve Stimulator To Treat Fibromyalgia Symptoms

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: 2026-01-19
• Device Publish Date: 2026-01-09

Devices Manufactured by NeuroMetrix, Inc.

• 00851221006780 - Quell Charger Cable: 2026-01-19Quell Charger Cable
• 00851221006780 - Quell Charger Cable: 2026-01-19 Quell Charger Cable
• 00851221006797 - Quell Charger Adapter: 2026-01-19 Quell Charger Adapter
• 00851221006056 - DPNCheck 2.0: 2026-01-12 DPNCheck 2.0 Device
• 00851221006575 - DPNCheck, China: 2026-01-12 DPNCheck Device, China
• 00851221006582 - DPNCheck, Japan: 2026-01-12 DPNCheck Device, Japan
• 00851221006513 - Quell Fibromyalgia: 2025-08-11 Standard Band for 2.0 Device
• 00851221006520 - Quell Fibromyalgia: 2025-08-11 Quell 12-Month Electrode Kit (Regular) - 12 sleeves of Electrodes
• 00851221006551 - Quell Fibromyalgia: 2025-08-11 Quell 12-Month Electrode Kit (Sport)