GUDIDData
eudamed_udi Primary ID: 03666256011107

Piège à eau parallèle, 22M-22M, adulte (UDI 03666256011107)

Manufactured by Int'Air Médical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Piège à eau parallèle, 22M-22M, adulte - Primary ID 03666256011107

Device Regulatory Overview

The Piège à eau parallèle, 22M-22M, adulte (Model/Catalog Number: AC54) is a medical device manufactured by Int'Air Médical. This product is indexed under FDA Product Code / Category Classification R028003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AC54
Product Code / EMDN
R028003
Device Name
Accessoires de circuits de ventilation non stériles
Database Sync Date
2026-08-09 18:29:39

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 Piège à eau parallèle, 22M-22M, adulte?

The registered manufacturer of record for Piège à eau parallèle, 22M-22M, adulte is Int'Air Médical.

What is the Primary UDI-DI identifier for Piège à eau parallèle, 22M-22M, adulte?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03666256011107.

What classification code is assigned to this device?

This device is registered under product classification code R028003.

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