GUDIDData
eudamed_udi Primary ID: 03666256013859

Cathéter mount tube intérieur lisse 22F-22M/15F double rotule bouchon double, filtre HME, adulte, 15cm (UDI 03666256013859)

Manufactured by Int'Air Médical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cathéter mount tube intérieur lisse 22F-22M/15F double rotule bouchon double, filtre HME, adulte, 15cm - Primary ID 03666256013859

Device Regulatory Overview

The Cathéter mount tube intérieur lisse 22F-22M/15F double rotule bouchon double, filtre HME, adulte, 15cm (Model/Catalog Number: CML03HME20A) is a medical device manufactured by Int'Air Médical. This product is indexed under FDA Product Code / Category Classification R020202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CML03HME20A
Product Code / EMDN
R020202
Device Name
Cathéters mount non stériles
Database Sync Date
2026-08-09 16:49:52

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 Cathéter mount tube intérieur lisse 22F-22M/15F double rotule bouchon double, filtre HME, adulte, 15cm?

The registered manufacturer of record for Cathéter mount tube intérieur lisse 22F-22M/15F double rotule bouchon double, filtre HME, adulte, 15cm is Int'Air Médical.

What is the Primary UDI-DI identifier for Cathéter mount tube intérieur lisse 22F-22M/15F double rotule bouchon double, filtre HME, adulte, 15cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03666256013859.

What classification code is assigned to this device?

This device is registered under product classification code R020202.

Programmatic Export

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

JSON API Endpoint