Australia TGA ARTG recordMINT Sterile single use absorbable polydioxanone suture with needle - Suture, polydioxanone
Australia TGA ARTG Registered Device · Hans Biomed Australia Pty Ltd · Hyundae Meditech Co Ltd · Class III · Started December 18, 2020
Good Name: Hans Biomed Australia Pty Ltd - MINT Sterile single use absorbable polydioxanone suture with needle - Suture, polydioxanone
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- December 18, 2020
- Effective Date
- December 18, 2020
- Country
- South Korea
- Address
- 80 Cheongjeong-ro Jijeong-myeon, Wonju-si, Gangwon-do, 26347
This device is intended to fixate sub dermal tissue in an elevated position in plastic and reconstructive surgery. The device is designed for minimally invasive face and neck application and is used in case of: - Slight and moderate skin laxity, soft tissue ptosis (without excessive skin volume) - Age-related neck changes, caused by atrophic processes of skin - Atrophic changes or uneven surface of skin and subdermal soft tissues
Access comprehensive regulatory information for MINT Sterile single use absorbable polydioxanone suture with needle - Suture, polydioxanone in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Hans Biomed Australia Pty Ltd, manufactured by Hyundae Meditech Co Ltd in South Korea. The device registration started on December 18, 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.