Austofix Intramedullary Nailing System (UDI 09339430008272)
Manufactured by Australian Orthopaedic Fixations Pty. Ltd.
Device Regulatory Overview
The Austofix Intramedullary Nailing System (Model/Catalog Number: 371240R) is a medical device manufactured by Australian Orthopaedic Fixations Pty. Ltd.. This product is indexed under FDA Product Code / Category Classification P09120201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 371240R
- Product Code / EMDN
- P09120201
- Device Name
- F3 Femoral Nail 125 Deg | 12 x 400mm RIGHT
- Database Sync Date
- 2026-08-09 16:28:48
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)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 09339430008272.
What classification code is assigned to this device?
This device is registered under product classification code P09120201.
Similar Classification Devices (P09120201)
Other Devices by Australian Orthopaedic Fixations Pty. Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint