GUDIDData
eudamed_udi Primary ID: 03760426520069

Chambre d’inhalation EG -9 mois (UDI 03760426520069)

Manufactured by Velmedys

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Chambre d’inhalation EG -9 mois - Primary ID 03760426520069

Device Regulatory Overview

The Chambre d’inhalation EG -9 mois (Model/Catalog Number: MDN1203) is a medical device manufactured by Velmedys. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MDN1203
Product Code / EMDN
R03010302
Device Name
Spacer for aerosol
Database Sync Date
2026-08-09 16:30:14

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 Chambre d’inhalation EG -9 mois?

The registered manufacturer of record for Chambre d’inhalation EG -9 mois is Velmedys.

What is the Primary UDI-DI identifier for Chambre d’inhalation EG -9 mois?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760426520069.

What classification code is assigned to this device?

This device is registered under product classification code R03010302.

Programmatic Export

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

JSON API Endpoint