GUDIDData
eudamed_udi Primary ID: 03665155001387

ERGODYNAMIC L (UDI 03665155001387)

Manufactured by FDI FRANCE

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERGODYNAMIC L - Primary ID 03665155001387

Device Regulatory Overview

The ERGODYNAMIC L (Model/Catalog Number: EDL/02/06) is a medical device manufactured by FDI FRANCE. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EDL/02/06
Product Code / EMDN
Y12030601
Device Name
Canne anglaise
Database Sync Date
2026-08-09 17:20:11

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 ERGODYNAMIC L?

The registered manufacturer of record for ERGODYNAMIC L is FDI FRANCE.

What is the Primary UDI-DI identifier for ERGODYNAMIC L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665155001387.

What classification code is assigned to this device?

This device is registered under product classification code Y12030601.

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