Pain Management

GUDID 04719871184721

Cutaneous Electrode Pad

EVERYWAY MEDICAL INSTRUMENTS CO., LTD.

Transcutaneous electrical stimulation electrode, reusable

• Primary Device ID: 04719871184721
• NIH Device Record Key: 98995572-dc05-4746-bf7c-da51c41d5a8a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pain Management
• Version Model Number: FA3000
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	04719871184721 [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: 2022-04-25
• Device Publish Date: 2022-04-15

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