gudid Primary ID: 08-0003

Adult Nasal Cannula for GI Source (UDI 08-0003)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Adult Nasal Cannula for GI Source (Model/Catalog Number: 08-0003) 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: 08-0003
Product Code / EMDN: CAT
Device Name: Adult Nasal Cannula, 10' O2/CO2 Sampling Line w/Male Luer
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 Adult Nasal Cannula for GI Source?

The registered manufacturer of record for Adult Nasal Cannula for GI Source is WESTMED, INC..

What is the Primary UDI-DI identifier for Adult Nasal Cannula for GI Source?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08-0003.

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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