WALKER SHORT NOIR (UDI 04719894924274)
Manufactured by e-life International Co., Ltd.
Device Regulatory Overview
The WALKER SHORT NOIR (Model/Catalog Number: 6754/ MWKUN03 (T4/ 43-46)) is a medical device manufactured by e-life International Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6754/ MWKUN03 (T4/ 43-46)
- Product Code / EMDN
- Y06120601
- Device Name
- Ankle/foot orthosis
- Database Sync Date
- 2026-08-09 16:29:23
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 WALKER SHORT NOIR?
The registered manufacturer of record for WALKER SHORT NOIR is e-life International Co., Ltd..
What is the Primary UDI-DI identifier for WALKER SHORT NOIR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719894924274.
What classification code is assigned to this device?
This device is registered under product classification code Y06120601.
Similar Classification Devices (Y06120601)
Other Devices by e-life International Co., Ltd.
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