GUDIDData
eudamed_udi Primary ID: 04719872867371

WellBind Thumb Brace (UDI 04719872867371)

Manufactured by Zhangpu Ortholife Rehabilitation Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WellBind Thumb Brace - Primary ID 04719872867371

Device Regulatory Overview

The WellBind Thumb Brace (Model/Catalog Number: 413002(S/M/UNI/Black)) is a medical device manufactured by Zhangpu Ortholife 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 16:28:59

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of WellBind Thumb Brace?

The registered manufacturer of record for WellBind Thumb Brace is Zhangpu Ortholife 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 04719872867371.

What classification code is assigned to this device?

This device is registered under product classification code Y060612.

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