eudamed_udi
Primary ID: 03665012001390
attelle de poignet ambidextre XL (UDI 03665012001390)
Manufactured by ORTHOMEDICA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for attelle de poignet ambidextre XL - Primary ID 03665012001390
Device Regulatory Overview
The attelle de poignet ambidextre XL (Model/Catalog Number: AP4) is a medical device manufactured by ORTHOMEDICA. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AP4
- Product Code / EMDN
- Y060612
- Device Name
- ATTELLE POIGNET
- Database Sync Date
- 2026-08-09 16:29:21
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 attelle de poignet ambidextre XL?
The registered manufacturer of record for attelle de poignet ambidextre XL is ORTHOMEDICA.
What is the Primary UDI-DI identifier for attelle de poignet ambidextre XL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665012001390.
What classification code is assigned to this device?
This device is registered under product classification code Y060612.
Similar Classification Devices (Y060612)
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