GUDIDData
eudamed_udi Primary ID: 09339430007220

Austofix Intramedullary Nailing System (UDI 09339430007220)

Manufactured by Australian Orthopaedic Fixations Pty. Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Austofix Intramedullary Nailing System - Primary ID 09339430007220

Device Regulatory Overview

The Austofix Intramedullary Nailing System (Model/Catalog Number: 366570) is a medical device manufactured by Australian Orthopaedic Fixations Pty. Ltd.. This product is indexed under FDA Product Code / Category Classification P09120604 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
366570
Product Code / EMDN
P09120604
Device Name
Hip Screw | 6.5 x 70mm
Database Sync Date
2026-08-09 16:29:19

Full Regulatory Attributes

đź”’ 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 Austofix Intramedullary Nailing System?

The registered manufacturer of record for Austofix Intramedullary Nailing System is Australian Orthopaedic Fixations Pty. Ltd..

What is the Primary UDI-DI identifier for Austofix Intramedullary Nailing System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09339430007220.

What classification code is assigned to this device?

This device is registered under product classification code P09120604.

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