GUDIDData
eudamed_udi Primary ID: 00619498149803

AIR TUBING - GREY 3 METRE. (UDI 00619498149803)

Manufactured by ResMed PTY LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIR TUBING - GREY 3 METRE. - Primary ID 00619498149803

Device Regulatory Overview

The AIR TUBING - GREY 3 METRE. (Model/Catalog Number: 14980) is a medical device manufactured by ResMed PTY LTD. This product is indexed under FDA Product Code / Category Classification R02010401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
14980
Product Code / EMDN
R02010401
Device Name
Air10 Tubing Elbow,Reusable Breathing Tubes,SlimLine Tube
Database Sync Date
2026-08-09 16:58:36

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 AIR TUBING - GREY 3 METRE.?

The registered manufacturer of record for AIR TUBING - GREY 3 METRE. is ResMed PTY LTD.

What is the Primary UDI-DI identifier for AIR TUBING - GREY 3 METRE.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00619498149803.

What classification code is assigned to this device?

This device is registered under product classification code R02010401.

Programmatic Export

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

JSON API Endpoint