gudid Primary ID: 1002350

Nebulizers (UDI 1002350)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nebulizers (Model/Catalog Number: 1002350) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1002350
Product Code / EMDN: CAF
Device Name: Small Volume Nebulizer Anti-Spill T MouthpieceW/7' Kink Resistant Tubing Standard Connector
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 Nebulizers?

The registered manufacturer of record for Nebulizers is WESTMED, INC..

What is the Primary UDI-DI identifier for Nebulizers?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1002350.

What classification code is assigned to this device?

This device is registered under product classification code CAF.

Similar Classification Devices (CAF)

Other Devices by WESTMED, INC.

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