Pro Ankle Brace (UDI 04712302982842)
Manufactured by e-life International Co., Ltd.
Device Regulatory Overview
The Pro Ankle Brace (Model/Catalog Number: MAN0060 (S/UNI/BK)) 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
- MAN0060 (S/UNI/BK)
- Product Code / EMDN
- Y06120601
- Device Name
- Ankle/foot orthosis and tubular support bandage
- Database Sync Date
- 2026-08-09 16:29:32
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 Pro Ankle Brace?
The registered manufacturer of record for Pro Ankle Brace is e-life International Co., Ltd..
What is the Primary UDI-DI identifier for Pro Ankle Brace?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712302982842.
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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