gudid
Primary ID: FAF2000
Pain Management (UDI FAF2000)
Manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pain Management - Primary ID FAF2000
Device Regulatory Overview
The Pain Management (Model/Catalog Number: FAF2000) is a medical device manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.. This product is indexed under FDA Product Code / Category Classification GXY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FAF2000
- Product Code / EMDN
- GXY
- Device Name
- Cutaneous Electrode Pad
- Database Sync Date
- 2026-08-09 09:06:39
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Pain Management?
The registered manufacturer of record for Pain Management is EVERYWAY MEDICAL INSTRUMENTS CO., LTD..
What is the Primary UDI-DI identifier for Pain Management?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FAF2000.
What classification code is assigned to this device?
This device is registered under product classification code GXY.
Similar Classification Devices (GXY)
Other Devices by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
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