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ReActiv8 Activator - Implantable lumbar neuromuscular electrical stimulation system control unit

Access comprehensive regulatory information for ReActiv8 Activator - Implantable lumbar neuromuscular electrical stimulation system control unit in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Mainstay Medical Australia Pty Ltd, manufactured by Mainstay Medical Limited in Ireland. The device registration started on December 04, 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
ReActiv8 Activator - Implantable lumbar neuromuscular electrical stimulation system control unit
Australia TGA ARTG Registered Device
Good Name: Mainstay Medical Australia Pty Ltd - ReActiv8 Activator - Implantable lumbar neuromuscular electrical stimulation system control unit
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Intended Purpose

An electronic component of an implantable lumbar neuromuscular electrical stimulation system (Reactiv8) intended to be used by a patient to telemetrically control its function (on/off) and delivery of treatment cycles. The ReActiv8 System is indicated as an aid in the management of intractable chronic low back pain associated with multifidus muscle dysfunction, as evidenced by imaging or physiological testing. It should only be used in cases of chronic low back pain despite medical management and attempting at least one course of physical therapy.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 04, 2019
Effective Date
December 04, 2019
Manufacturer
Country
Ireland
Address
Clonmel House Forster Way Swords, Co Dublin, K67F2k3