Everyway (UDI EM-6300 (Li-battery))
Manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Device Regulatory Overview
The Everyway (Model/Catalog Number: EM-6300 (Li-battery)) is a medical device manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.. This product is indexed under FDA Product Code / Category Classification NUH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EM-6300 (Li-battery)
- Product Code / EMDN
- NUH
- Device Name
- Electrical Muscel Stimulator (EMS)
- 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 EM-6300 (Li-battery).
What classification code is assigned to this device?
This device is registered under product classification code NUH.
Similar Classification Devices (NUH)
Other Devices by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
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