gudid Primary ID: 3120-E

Adult Venturi Elongated Mask Kit (UDI 3120-E)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Adult Venturi Elongated Mask Kit (Model/Catalog Number: 3120-E) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification BYF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 3120-E
Product Code / EMDN: BYF
Device Name: Adult Venturi Elongated Mask Kit w/All Diluters,7' Tube w/TN
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 Venturi Elongated Mask Kit?

The registered manufacturer of record for Adult Venturi Elongated Mask Kit is WESTMED, INC..

What is the Primary UDI-DI identifier for Adult Venturi Elongated Mask Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3120-E.

What classification code is assigned to this device?

This device is registered under product classification code BYF.

Similar Classification Devices (BYF)

Other Devices by WESTMED, INC.

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