GUDIDData
eudamed_udi Primary ID: 03770039895003

Elo-D (UDI 03770039895003)

Manufactured by ELODIE SAS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Elo-D - Primary ID 03770039895003

Device Regulatory Overview

The Elo-D (Model/Catalog Number: Kit complet - taille 0) is a medical device manufactured by ELODIE SAS. This product is indexed under FDA Product Code / Category Classification Y120380 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Kit complet - taille 0
Product Code / EMDN
Y120380
Device Name
Shock absorber kit for medical crutch
Database Sync Date
2026-08-09 16:29:46

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 Elo-D?

The registered manufacturer of record for Elo-D is ELODIE SAS.

What is the Primary UDI-DI identifier for Elo-D?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770039895003.

What classification code is assigned to this device?

This device is registered under product classification code Y120380.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint