gudid Primary ID: 0312

Nebulizer (UDI 0312)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nebulizer (Model/Catalog Number: 0312) 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: 0312
Product Code / EMDN: CAF
Device Name: VixOneTM Nebulizer with Super Spike Mask
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 Nebulizer?

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

What is the Primary UDI-DI identifier for Nebulizer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0312.

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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