WellBind Thumb Brace (UDI 04719964461982)
Manufactured by Orthotech Rehabilitation Co., Ltd.
Device Regulatory Overview
The WellBind Thumb Brace (Model/Catalog Number: 413002(S/M/UNI/Black)) is a medical device manufactured by Orthotech Rehabilitation Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 413002(S/M/UNI/Black)
- Product Code / EMDN
- Y060612
- Device Name
- Wrist Splint (Wrist orthosis)
- Database Sync Date
- 2026-08-09 16:29:06
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 WellBind Thumb Brace?
The registered manufacturer of record for WellBind Thumb Brace is Orthotech Rehabilitation Co., Ltd..
What is the Primary UDI-DI identifier for WellBind Thumb Brace?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719964461982.
What classification code is assigned to this device?
This device is registered under product classification code Y060612.
Similar Classification Devices (Y060612)
Other Devices by Orthotech Rehabilitation Co., Ltd.
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