eudamed_udi
Primary ID: 04719871183274
Everyway (UDI 04719871183274)
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 04719871183274
Device Regulatory Overview
The Everyway (Model/Catalog Number: HC-881A) is a medical device manufactured by Everyway Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HC-881A
- Product Code / EMDN
- Z12062899
- Device Name
- Conductive Garments
- Database Sync Date
- 2026-08-09 17:20:56
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 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 04719871183274.
What classification code is assigned to this device?
This device is registered under product classification code Z12062899.
Similar Classification Devices (Z12062899)
Other Devices by Everyway Medical Instrument Co., Ltd.
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