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Timpel Enlight Electrical Impedance Tomography - Thoracic electrical bioimpedance system electrode array, reusable - ARTG 457826

Access comprehensive regulatory information for Timpel Enlight Electrical Impedance Tomography - Thoracic electrical bioimpedance system electrode array, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 457826 and sponsored by Bellavista Medical ANZ Pty Ltd, manufactured by Timpel S A in Brazil. The device registration started on July 31, 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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Class I
ARTG 457826
Class I
Timpel Enlight Electrical Impedance Tomography - Thoracic electrical bioimpedance system electrode array, reusable
ARTG ID: 457826
Good Name: Bellavista Medical ANZ Pty Ltd - Timpel Enlight Electrical Impedance Tomography - Thoracic electrical bioimpedance system electrode array, reusable
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Intended Purpose

The Reusable Timpel Enlight Electrode belt is used to apply & acquire a patient's electrical impedance signals across the thoracic chest, in different patient sizes for the purpose of mapping regional ventilation of a patient's lungs.

Device Classification
Risk Class
Class I
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
457826
Start Date
July 31, 2024
Effective Date
July 31, 2024
Manufacturer
Country
Brazil
Address
Rua Jose Leonardi 280 Bloco A, Aeroporto, Pato Branco, Parana, 85 503-000