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PURISMA PLASMALIFT - Radio-frequency skin surface treatment system

Australia TGA ARTG Registered Device · MM Beauty Equipment Services Pty Ltd · Daeyang Medical Co Ltd · Class IIb · Started July 20, 2020

Good Name: MM Beauty Equipment Services Pty Ltd - PURISMA PLASMALIFT - Radio-frequency skin surface treatment system

Device classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration information
Start Date
July 20, 2020
Effective Date
July 20, 2020
Sponsor
Manufacturer
Country
South Korea
Address
147 Donghwakongdan-ro Donghwa-ri, Munmak-eup, Wonju-si, Gangwon-do
Intended purpose

Purisma Plasmalift skin surface treatment RF system is indicated for : scar reduction, skin tightening and lifting, fine line reduction, stretch mark reduction, skin lifting, acne treatment, eyelid lifting, skin toning, skin sterilisation, reduction of pores and regeneration, acne reduction by skin surface sterilization, general skin tone up by emitting high plasma energy over a wide range of the skin

About this record

Access comprehensive regulatory information for PURISMA PLASMALIFT - Radio-frequency skin surface treatment system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by MM Beauty Equipment Services Pty Ltd, manufactured by Daeyang Medical Co Ltd in South Korea. The device registration started on July 20, 2020.

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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