eudamed_udi
Primary ID: 04719871185315
Everyway (UDI 04719871185315)
Manufactured by Everyway Medical Instrument Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Everyway - Primary ID 04719871185315
Device Regulatory Overview
The Everyway (Model/Catalog Number: KF100152) is a medical device manufactured by Everyway Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification N010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KF100152
- Product Code / EMDN
- N010201
- Device Name
- Cutaneous Electrode Pad
- Database Sync Date
- 2026-08-09 16:46:16
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 Instrument Co., Ltd..
What is the Primary UDI-DI identifier for Everyway?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719871185315.
What classification code is assigned to this device?
This device is registered under product classification code N010201.
Similar Classification Devices (N010201)
Other Devices by Everyway Medical Instrument Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint