eudamed_udi
Primary ID: 05690977311275
Rebound® Ankle Brace (UDI 05690977311275)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rebound® Ankle Brace - Primary ID 05690977311275
Device Regulatory Overview
The Rebound® Ankle Brace (Model/Catalog Number: B-231502514) is a medical device manufactured by Össur Iceland ehf.. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B-231502514
- Product Code / EMDN
- Y06120601
- Device Name
- BU00029
- Database Sync Date
- 2026-08-09 16:28:58
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 Rebound® Ankle Brace?
The registered manufacturer of record for Rebound® Ankle Brace is Össur Iceland ehf..
What is the Primary UDI-DI identifier for Rebound® Ankle Brace?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690977311275.
What classification code is assigned to this device?
This device is registered under product classification code Y06120601.
Similar Classification Devices (Y06120601)
Other Devices by Össur Iceland ehf.
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