Pneumatic Walker (UDI 04712302988943)
Manufactured by e-life International Co., Ltd.
Device Regulatory Overview
The Pneumatic Walker (Model/Catalog Number: MWKFS01 (L/UNI/GY/11)) 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
- MWKFS01 (L/UNI/GY/11)
- Product Code / EMDN
- Y06120601
- Device Name
- Ankle/foot orthosis
- Database Sync Date
- 2026-08-09 16:29:38
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 Pneumatic Walker?
The registered manufacturer of record for Pneumatic Walker is e-life International Co., Ltd..
What is the Primary UDI-DI identifier for Pneumatic Walker?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712302988943.
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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