GUDIDData
gudid Primary ID: 01.24.308

Mfinity Femoral System (UDI 01.24.308)

Manufactured by Medacta International SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mfinity Femoral System - Primary ID 01.24.308

Device Regulatory Overview

The Mfinity Femoral System (Model/Catalog Number: 01.24.308) is a medical device manufactured by Medacta International SA. This product is indexed under FDA Product Code / Category Classification MEH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
01.24.308
Product Code / EMDN
MEH
Device Name
M-Finity collared stem size 8 STD
Database Sync Date
2026-08-09 09:03:14

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 Mfinity Femoral System?

The registered manufacturer of record for Mfinity Femoral System is Medacta International SA.

What is the Primary UDI-DI identifier for Mfinity Femoral System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01.24.308.

What classification code is assigned to this device?

This device is registered under product classification code MEH.

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