Pain Management

GUDID 04719871186008

Cutaneous Electrode Pad

EVERYWAY MEDICAL INSTRUMENTS CO., LTD.

Transcutaneous electrical stimulation electrode, reusable

• Primary Device ID: 04719871186008
• NIH Device Record Key: 2135097d-b955-401c-857b-6f195ee8aa4b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pain Management
• Version Model Number: TR2020
• Company DUNS: 657383535
• Company Name: EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719871186008 [Primary]

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2025-08-28
• Device Publish Date: 2025-08-20

On-Brand Devices [Pain Management]

• 04719871184752: Cutaneous Electrode Pad
• 04719871184745: Cutaneous Electrode Pad
• 04719871184738: Cutaneous Electrode Pad
• 04719871184721: Cutaneous Electrode Pad
• 04719871184714: Cutaneous Electrode Pad
• 04719871184707: Cutaneous Electrode Pad
• 04719871186008: Cutaneous Electrode Pad
• 04719871185995: Cutaneous Electrode Pad
• 04719871185988: Cutaneous Electrode Pad
• 04719871185971: Cutaneous Electrode Pad