gudid Primary ID: VM-98020

VENTURI MASK CHILD W/7 DILUTERS , W/7FT TUBING, 6 INCH CORRUGATE TUBE (UDI VM-98020)

Manufactured by BESMED HEALTH BUSINESS CORP.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VENTURI MASK CHILD W/7 DILUTERS , W/7FT TUBING, 6 INCH CORRUGATE TUBE (Model/Catalog Number: VM-98020) is a medical device manufactured by BESMED HEALTH BUSINESS CORP.. This product is indexed under FDA Product Code / Category Classification BYF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VM-98020
Product Code / EMDN: BYF
Device Name: VENTURI MASK CHILD W/7 DILUTERS , W/7FT TUBING, 6 INCH CORRUGATE TUBE
Database Sync Date: 2026-08-09 09:15:29

Full Regulatory Attributes

🔒 Token Gated

{
    "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 VENTURI MASK CHILD W/7 DILUTERS , W/7FT TUBING, 6 INCH CORRUGATE TUBE?

The registered manufacturer of record for VENTURI MASK CHILD W/7 DILUTERS , W/7FT TUBING, 6 INCH CORRUGATE TUBE is BESMED HEALTH BUSINESS CORP..

What is the Primary UDI-DI identifier for VENTURI MASK CHILD W/7 DILUTERS , W/7FT TUBING, 6 INCH CORRUGATE TUBE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VM-98020.

What classification code is assigned to this device?

This device is registered under product classification code BYF.

Similar Classification Devices (BYF)

Other Devices by BESMED HEALTH BUSINESS CORP.

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