eudamed_udi
Primary ID: 03700437216360
HEXAGON (UDI 03700437216360)
Manufactured by EUROS SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HEXAGON - Primary ID 03700437216360
Device Regulatory Overview
The HEXAGON (Model/Catalog Number: A311525151) is a medical device manufactured by EUROS SAS. This product is indexed under FDA Product Code / Category Classification P090903020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A311525151
- Product Code / EMDN
- P090903020202
- Device Name
- HEXAGON
- Database Sync Date
- 2026-08-09 16:28:47
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of HEXAGON?
The registered manufacturer of record for HEXAGON is EUROS SAS.
What is the Primary UDI-DI identifier for HEXAGON?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700437216360.
What classification code is assigned to this device?
This device is registered under product classification code P090903020202.
Similar Classification Devices (P090903020202)
Other Devices by EUROS SAS
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint