eudamed_udi Primary ID: 07611819681071

SYNFIX Evolution (UDI 07611819681071)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The SYNFIX Evolution (Model/Catalog Number: 03.835.243) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification Z12139099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 03.835.243
Product Code / EMDN: Z12139099
Device Name: SYNFIX Evolution Footprint Trial Trial Implant Small Medium Large
Database Sync Date: 2026-08-09 16:29:16

Full Regulatory Attributes

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{
    "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 SYNFIX Evolution?

The registered manufacturer of record for SYNFIX Evolution is Synthes GmbH.

What is the Primary UDI-DI identifier for SYNFIX Evolution?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611819681071.

What classification code is assigned to this device?

This device is registered under product classification code Z12139099.

Similar Classification Devices (Z12139099)

Other Devices by Synthes GmbH

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