eudamed_udi
Primary ID: 05690967140182
Iceross® Transfemoral Locking (UDI 05690967140182)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Iceross® Transfemoral Locking - Primary ID 05690967140182
Device Regulatory Overview
The Iceross® Transfemoral Locking (Model/Catalog Number: I-713236) is a medical device manufactured by Össur Iceland ehf.. This product is indexed under FDA Product Code / Category Classification Y062415 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- I-713236
- Product Code / EMDN
- Y062415
- Device Name
- BU00003
- Database Sync Date
- 2026-08-09 16:29:38
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 Iceross® Transfemoral Locking?
The registered manufacturer of record for Iceross® Transfemoral Locking is Össur Iceland ehf..
What is the Primary UDI-DI identifier for Iceross® Transfemoral Locking?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690967140182.
What classification code is assigned to this device?
This device is registered under product classification code Y062415.
Similar Classification Devices (Y062415)
Other Devices by Össur Iceland ehf.
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