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Biological Feedback and Stimulation System - Perineal orifice incontinence-control electrical stimulator, professional - ARTG 481705

Access comprehensive regulatory information for Biological Feedback and Stimulation System - Perineal orifice incontinence-control electrical stimulator, professional in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 481705 and sponsored by Robin Healthcare Pty Ltd, manufactured by Medlander Medical Technology Inc in China. The device registration started on March 05, 2025.

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 IIa
ARTG 481705
Class IIa
Biological Feedback and Stimulation System - Perineal orifice incontinence-control electrical stimulator, professional
ARTG ID: 481705
Good Name: Robin Healthcare Pty Ltd - Biological Feedback and Stimulation System - Perineal orifice incontinence-control electrical stimulator, professional
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Intended Purpose

Biological Feedback and Stimulation System is a medical device designed to be used in the hospital and clinic healthcare environment to treat symptoms of urinary and/or faecal incontinence and help to relieve symptoms of chronic pelvic pain.

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
481705
Start Date
March 05, 2025
Effective Date
March 05, 2025
Manufacturer
Country
China
Address
Building 5 Acceleration Zone Nanjing Life Science and Technology Innovation Park, No 6 Qiande Road Jiangning District, Nanjing, Jiangsu, 211100