gudid Primary ID: 0920

CO2/O2 Nasal Cannula (UDI 0920)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The CO2/O2 Nasal Cannula (Model/Catalog Number: 0920) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 0920
Product Code / EMDN: CAT
Device Name: Adult Nasal Cannula, 7' CO2/O2 w Reflective Luer, Gas Sampling Tee and Comfort Soft Plus Tubing
Database Sync Date: 2026-08-09 09:04:13

Full Regulatory Attributes

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{
    "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 CO2/O2 Nasal Cannula?

The registered manufacturer of record for CO2/O2 Nasal Cannula is WESTMED, INC..

What is the Primary UDI-DI identifier for CO2/O2 Nasal Cannula?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0920.

What classification code is assigned to this device?

This device is registered under product classification code CAT.

Similar Classification Devices (CAT)

Other Devices by WESTMED, INC.

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