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AXONICS SNM SYSTEM™ Clinician Programmer 2501 - Incontinence-control electrical stimulation system programmer

Access comprehensive regulatory information for AXONICS SNM SYSTEM™ Clinician Programmer 2501 - Incontinence-control electrical stimulation system programmer in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Axonics Modulation Technologies Australia Pty Ltd, manufactured by Axonics Inc in United States of America. The device registration started on November 06, 2019.

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
Class III
AXONICS SNM SYSTEM™ Clinician Programmer 2501 - Incontinence-control electrical stimulation system programmer
Australia TGA ARTG Registered Device
Good Name: Axonics Modulation Technologies Australia Pty Ltd - AXONICS SNM SYSTEM™ Clinician Programmer 2501 - Incontinence-control electrical stimulation system programmer
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Intended Purpose

The AXONICS SNM SYSTEM™ Clinician Programmer is a nonimplantable accessory to the nonimplantable AXONICS SNM SYSTEM Trial Stimulator and to the Axonics Neurostimulator AIMD, both of which are intended to treat urinary and/or faecal incontinence. The clinician programmer is a custom tablet computer used by a clinician to facilitate lead placement; program an implantable neurostimulator or a nonimplantable trial stimulator; deliver test stimulation.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
November 06, 2019
Effective Date
November 06, 2019
Manufacturer
Country
United States of America
Address
26 Technology Drive, Irvine, California, 92618