GUDIDData
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eudamed_udi Primary ID: 03700437215189

HEXAGON (UDI 03700437215189)

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 03700437215189

Device Regulatory Overview

The HEXAGON (Model/Catalog Number: A311211081) is a medical device manufactured by EUROS SAS. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
A311211081
Product Code / EMDN
P0909030101
Device Name
HEXAGON
Database Sync Date
2026-08-09 16:30:11

Full Regulatory Attributes

🔒 Token Gated 
{
    "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 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 03700437215189.

What classification code is assigned to this device?

This device is registered under product classification code P0909030101.

Similar Classification Devices (P0909030101)

Other Devices by EUROS SAS

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