Australia flagARTG 381671

Saebo Stim Pro - Analgesic TENS system

ARTG ID: 381671 · Ausmedic Australia Pty Ltd · Shenzhen XFT Medical Limited · Class IIa · Started January 04, 2022

Good Name: Ausmedic Australia Pty Ltd - Saebo Stim Pro - Analgesic TENS system

Device classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration information
ARTG ID
381671
Start Date
January 04, 2022
Effective Date
January 04, 2022
Sponsor
Manufacturer
Country
China
Address
Room 203 Building 1 Biomedicine Innovations Industrial Park #14 Jinhui Road, Pingshan New District, Shenzhen, 518122
Intended purpose

A device intended to deliver muscle and nerve stimulation using the principles of both Neuromuscular Electrical Stimulation (NMES) and Transcutaneous Electrical Nerve Stimulation (TENS).

About this record

Access comprehensive regulatory information for Saebo Stim Pro - Analgesic TENS system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 381671 and sponsored by Ausmedic Australia Pty Ltd, manufactured by Shenzhen XFT Medical Limited in China. The device registration started on January 04, 2022.

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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