GUDIDData
eudamed_udi Primary ID: 03666256012838

Système manuel de contrôle d'aspiration vert avec crochet, tubulure 2.50m adulte (UDI 03666256012838)

Manufactured by Int'Air Médical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Système manuel de contrôle d'aspiration vert avec crochet, tubulure 2.50m adulte - Primary ID 03666256012838

Device Regulatory Overview

The Système manuel de contrôle d'aspiration vert avec crochet, tubulure 2.50m adulte (Model/Catalog Number: D3065) is a medical device manufactured by Int'Air Médical. This product is indexed under FDA Product Code / Category Classification R0580 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
D3065
Product Code / EMDN
R0580
Device Name
Dispositifs et accessoires d'aspiration non stériles
Database Sync Date
2026-08-09 16:29:04

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 Système manuel de contrôle d'aspiration vert avec crochet, tubulure 2.50m adulte?

The registered manufacturer of record for Système manuel de contrôle d'aspiration vert avec crochet, tubulure 2.50m adulte is Int'Air Médical.

What is the Primary UDI-DI identifier for Système manuel de contrôle d'aspiration vert avec crochet, tubulure 2.50m adulte?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03666256012838.

What classification code is assigned to this device?

This device is registered under product classification code R0580.

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