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Disposable Intraoperative Probe - Invasive/noninvasive vascular ultrasound probe - ARTG 465126

Access comprehensive regulatory information for Disposable Intraoperative Probe - Invasive/noninvasive vascular ultrasound probe in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 465126 and sponsored by Arjo Australia Pty Ltd, manufactured by ArjoHuntleigh AB in Sweden. The device registration started on October 21, 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 III
ARTG 465126
Class III
Disposable Intraoperative Probe - Invasive/noninvasive vascular ultrasound probe
ARTG ID: 465126
Good Name: Arjo Australia Pty Ltd - Disposable Intraoperative Probe - Invasive/noninvasive vascular ultrasound probe
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Intended Purpose

The DIOP8 surgical Doppler is indicated for use by qualified healthcare practitioners in a sterile condition in the operating theatre for the assessment of vascular blood flow by direct application to the vessel wall. The DIOP8 is suitable for use on all patient populations.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
465126
Start Date
October 21, 2024
Effective Date
October 21, 2024
Manufacturer
Country
Sweden
Address
Hans Michelsensgatan 10, Malmo, 21120