eudamed_udi
Primary ID: 04710374235118
Genu-Knit Brace (UDI 04710374235118)
Manufactured by e-life International Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Genu-Knit Brace - Primary ID 04710374235118
Device Regulatory Overview
The Genu-Knit Brace (Model/Catalog Number: MKNK202 (S/UNI/GY)) is a medical device manufactured by e-life International Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MKNK202 (S/UNI/GY)
- Product Code / EMDN
- Y061209
- Device Name
- Knee orthosis and tubular support bandage
- Database Sync Date
- 2026-08-09 16:29:19
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 Genu-Knit Brace?
The registered manufacturer of record for Genu-Knit Brace is e-life International Co., Ltd..
What is the Primary UDI-DI identifier for Genu-Knit Brace?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04710374235118.
What classification code is assigned to this device?
This device is registered under product classification code Y061209.
Similar Classification Devices (Y061209)
Other Devices by e-life International Co., Ltd.
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