ARTG 391093Perineal orifice incontinence-control electrical stimulator, home-use
ARTG ID: 391093 · ACRA Regulatory Services Pty Ltd · Verity Medical Ltd · Class IIa · Started June 22, 2022
Good Name: ACRA Regulatory Services Pty Ltd - Perineal orifice incontinence-control electrical stimulator, home-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 391093
- Start Date
- June 22, 2022
- Effective Date
- June 22, 2022
- Country
- Ireland
- Address
- Churchtown House, Tagoat, Co Wexford, Y35 XY44
A battery powered electrical stimulator intended to be used to stimulate the muscles and nerve fibres in the pelvic area and is indicated for use: pelvic pain, back pain, stress incontinence, overactive bladder and faecal incontinence
Access comprehensive regulatory information for Perineal orifice incontinence-control electrical stimulator, home-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 391093 and sponsored by ACRA Regulatory Services Pty Ltd, manufactured by Verity Medical Ltd in Ireland. The device registration started on June 22, 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.