eudamed_udi
Primary ID: 05690967566739
Iceross Seal-In® Transfemoral (UDI 05690967566739)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Iceross Seal-In® Transfemoral - Primary ID 05690967566739
Device Regulatory Overview
The Iceross Seal-In® Transfemoral (Model/Catalog Number: I-453225) 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-453225
- Product Code / EMDN
- Y062415
- Device Name
- BU00001
- Database Sync Date
- 2026-08-09 16:44:47
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 Seal-In® Transfemoral?
The registered manufacturer of record for Iceross Seal-In® Transfemoral is Össur Iceland ehf..
What is the Primary UDI-DI identifier for Iceross Seal-In® Transfemoral?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690967566739.
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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