gudid
Primary ID: MT-200
Everyway (UDI MT-200)
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 Everyway - Primary ID MT-200
Device Regulatory Overview
The Everyway (Model/Catalog Number: MT-200) is a medical device manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.. This product is indexed under FDA Product Code / Category Classification NFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MT-200
- Product Code / EMDN
- NFO
- Device Name
- Stimulator, transcutaneous electrical, aesthetic purposes
- Database Sync Date
- 2026-08-09 09:15:29
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 Everyway?
The registered manufacturer of record for Everyway is EVERYWAY MEDICAL INSTRUMENTS CO., LTD..
What is the Primary UDI-DI identifier for Everyway?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MT-200.
What classification code is assigned to this device?
This device is registered under product classification code NFO.
Similar Classification Devices (NFO)
Other Devices by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
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