Australia flagARTG 441152

Manual jet ventilation device

ARTG ID: 441152 · Lateral Medical · Ventinova Medical BV · Class IIa · Started February 15, 2024

Good Name: Lateral Medical - Manual jet ventilation device

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
441152
Start Date
February 15, 2024
Effective Date
February 15, 2024
Sponsor
Manufacturer
Country
Netherlands
Address
Meerenakkerplein 7, BJ Eindhoven, 5652
Intended purpose

Ventrain: ‘Ventrain is intended to be used for ventilation through a small bore lumen in patients with a difficult airway where conventional ventilation by mask and/or a large-bore endotracheal tube is not preferred’ Cricath: ‘Cricath Adult is intended for obtaining access to the trachea when conventional intubation by mask and/or large-bore endotracheal tube cannot be performed in adult patients’ Tritube: ‘Tritube is intended to be used for obtaining endotracheal access to the airway for ventilating a patient with an active expiration device with a contact duration for less than 24 hours with a single tube’

About this record

Access comprehensive regulatory information for Manual jet ventilation device in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 441152 and sponsored by Lateral Medical, manufactured by Ventinova Medical BV in Netherlands. The device registration started on February 15, 2024.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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