gudid Primary ID: 0236

VixOne (UDI 0236)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VixOne (Model/Catalog Number: 0236) 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: 0236
Product Code / EMDN: CAF
Device Name: VixOne, Infant Nebulizer Kit
Database Sync Date: 2026-08-09 09:04:13

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 VixOne?

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

What is the Primary UDI-DI identifier for VixOne?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0236.

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.

Programmatic Export

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

JSON API Endpoint