WellFit Wrist Brace (UDI 04719964463856)
Manufactured by Orthotech Rehabilitation Co., Ltd.
Device Regulatory Overview
The WellFit Wrist Brace (Model/Catalog Number: 410010(S/Left/Black)) is a medical device manufactured by Orthotech Rehabilitation Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y060609 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 410010(S/Left/Black)
- Product Code / EMDN
- Y060609
- Device Name
- Wrist Splint (Wrist orthosis)
- Database Sync Date
- 2026-08-09 16:28:56
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 WellFit Wrist Brace?
The registered manufacturer of record for WellFit Wrist Brace is Orthotech Rehabilitation Co., Ltd..
What is the Primary UDI-DI identifier for WellFit Wrist Brace?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719964463856.
What classification code is assigned to this device?
This device is registered under product classification code Y060609.
Similar Classification Devices (Y060609)
Other Devices by Orthotech Rehabilitation Co., Ltd.
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