eudamed_udi
Primary ID: 05690977253544
AeroFit® Socket (UDI 05690977253544)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AeroFit® Socket - Primary ID 05690977253544
Device Regulatory Overview
The AeroFit® Socket (Model/Catalog Number: AFS511176) 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
- AFS511176
- Product Code / EMDN
- Y062415
- Device Name
- BU00012
- Database Sync Date
- 2026-08-09 16:45:44
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 AeroFit® Socket?
The registered manufacturer of record for AeroFit® Socket is Össur Iceland ehf..
What is the Primary UDI-DI identifier for AeroFit® Socket?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690977253544.
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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