eudamed_udi
Primary ID: 05690977181694
Philadelphia Liner (UDI 05690977181694)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Philadelphia Liner - Primary ID 05690977181694
Device Regulatory Overview
The Philadelphia Liner (Model/Catalog Number: PHP-LCS) is a medical device manufactured by Össur Iceland ehf.. This product is indexed under FDA Product Code / Category Classification Y060380 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PHP-LCS
- Product Code / EMDN
- Y060380
- Device Name
- BU00085
- Database Sync Date
- 2026-08-09 16:45:40
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 Philadelphia Liner?
The registered manufacturer of record for Philadelphia Liner is Össur Iceland ehf..
What is the Primary UDI-DI identifier for Philadelphia Liner?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690977181694.
What classification code is assigned to this device?
This device is registered under product classification code Y060380.
Similar Classification Devices (Y060380)
Other Devices by Össur Iceland ehf.
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