eudamed_udi
Primary ID: 03700448201669
Eurofix VTP (UDI 03700448201669)
Manufactured by SYNERGIE INGENIERIE MEDICALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eurofix VTP - Primary ID 03700448201669
Device Regulatory Overview
The Eurofix VTP (Model/Catalog Number: 884108) is a medical device manufactured by SYNERGIE INGENIERIE MEDICALE. This product is indexed under FDA Product Code / Category Classification P099001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 884108
- Product Code / EMDN
- P099001
- Device Name
- Eurofix Cement for Vertebroplasty
- Database Sync Date
- 2026-08-09 16:59:57
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Eurofix VTP?
The registered manufacturer of record for Eurofix VTP is SYNERGIE INGENIERIE MEDICALE.
What is the Primary UDI-DI identifier for Eurofix VTP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700448201669.
What classification code is assigned to this device?
This device is registered under product classification code P099001.
Similar Classification Devices (P099001)
Other Devices by SYNERGIE INGENIERIE MEDICALE
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