eudamed_udi
Primary ID: 03700448200013
Biofix 1G (UDI 03700448200013)
Manufactured by SYNERGIE INGENIERIE MEDICALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Biofix 1G - Primary ID 03700448200013
Device Regulatory Overview
The Biofix 1G (Model/Catalog Number: 880225) 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
- 880225
- Product Code / EMDN
- P099001
- Device Name
- Biofix 1G: orthopedic cement with gentamicin
- Database Sync Date
- 2026-08-09 16:49:52
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 Biofix 1G?
The registered manufacturer of record for Biofix 1G is SYNERGIE INGENIERIE MEDICALE.
What is the Primary UDI-DI identifier for Biofix 1G?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700448200013.
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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