eudamed_udi
Primary ID: 07611819680418
SYNFIX Evolution (UDI 07611819680418)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SYNFIX Evolution - Primary ID 07611819680418
Device Regulatory Overview
The SYNFIX Evolution (Model/Catalog Number: 03.835.102) 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
- 03.835.102
- Product Code / EMDN
- Z12139099
- Device Name
- SYNFIX Evolution Footprint Trial Trial Implant Small Medium Large
- Database Sync Date
- 2026-08-09 16:29:30
Full Regulatory Attributes
đź”’ Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 07611819680418.
What classification code is assigned to this device?
This device is registered under product classification code Z12139099.
Similar Classification Devices (Z12139099)
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