eudamed_udi
Primary ID: 05690977472563
Posterior panels (UDI 05690977472563)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Posterior panels - Primary ID 05690977472563
Device Regulatory Overview
The Posterior panels (Model/Catalog Number: MLSO-P12) 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
- MLSO-P12
- Product Code / EMDN
- Y060380
- Device Name
- BU00081
- Database Sync Date
- 2026-08-09 16:44:53
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 Posterior panels?
The registered manufacturer of record for Posterior panels is Össur Iceland ehf..
What is the Primary UDI-DI identifier for Posterior panels?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690977472563.
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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