GUDIDData
eudamed_udi Primary ID: 08682076500084

Ortoknee (UDI 08682076500084)

Manufactured by ORTONOM MEDİKAL ÜRÜNLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ortoknee - Primary ID 08682076500084

Device Regulatory Overview

The Ortoknee (Model/Catalog Number: DZ0011) is a medical device manufactured by ORTONOM MEDİKAL ÜRÜNLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DZ0011
Product Code / EMDN
P0909030101
Device Name
Ortoknee CoCr PS Anatomic Femoral Component Cemented Right Size - F (3,5)-72mm
Database Sync Date
2026-08-09 16:29:15

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 Ortoknee?

The registered manufacturer of record for Ortoknee is ORTONOM MEDİKAL ÜRÜNLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ.

What is the Primary UDI-DI identifier for Ortoknee?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682076500084.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

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