Australia TGA ARTG record

Suture, polyethylene

Australia TGA ARTG Registered Device · Smith & Nephew Pty Ltd · Riverpoint Medical LLC · Class IIb · Started October 07, 2021

Good Name: Smith & Nephew Pty Ltd - Suture, polyethylene

Device classification

Risk Class: Class IIb
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: October 07, 2021
Effective Date: October 07, 2021

Sponsor

Name: Smith & Nephew Pty Ltd

Manufacturer

Name: Riverpoint Medical LLC
Country: United States of America
Address: 825 NE 25th Avenue, Portland, OR, 97232

Intended purpose

Intended for use in general soft tissue approximation and/or ligation and the use of allograft tissues for orthopedic surgeries.

About this record

Access comprehensive regulatory information for Suture, polyethylene in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Smith & Nephew Pty Ltd, manufactured by Riverpoint Medical LLC in United States of America. The device registration started on October 07, 2021.

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.