GUDIDData
eudamed_udi Primary ID: 05690967816674

OP4 Knee (UDI 05690967816674)

Manufactured by Össur Iceland ehf.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OP4 Knee - Primary ID 05690967816674

Device Regulatory Overview

The OP4 Knee (Model/Catalog Number: 1720185-L) 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
1720185-L
Product Code / EMDN
Y062415
Device Name
BU00055
Database Sync Date
2026-08-09 16:28:57

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of OP4 Knee?

The registered manufacturer of record for OP4 Knee is Össur Iceland ehf..

What is the Primary UDI-DI identifier for OP4 Knee?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690967816674.

What classification code is assigned to this device?

This device is registered under product classification code Y062415.

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