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Analgesic TENS system

Australia TGA ARTG Registered Device · RITM Australia Pty Ltd · TRONITEK LLC · Class IIa · Started August 19, 2019

Good Name: RITM Australia Pty Ltd - Analgesic TENS system

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
Start Date
August 19, 2019
Effective Date
August 19, 2019
Sponsor
Manufacturer
Country
Russia
Address
15 Akademika Postovskogo Str, Ekaterinburg, 620146
Intended purpose

SCENAR-Vertebra is a multipurpose Transcutaneous Electrical Neuro Stimulator designed for non-invasive therapeutic treatment of the segmental zones of the back to provide pain relief therapy and rehabilitation after surgery or trauma.

About this record

Access comprehensive regulatory information for Analgesic TENS system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by RITM Australia Pty Ltd, manufactured by TRONITEK LLC in Russia. The device registration started on August 19, 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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