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Suture, polyethylene

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.

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TGA ARTG Official Data
Class IIb
Class IIb
Suture, polyethylene
Australia TGA ARTG Registered Device
Good Name: Smith & Nephew Pty Ltd - Suture, polyethylene
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Intended Purpose

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

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
Manufacturer
Country
United States of America
Address
825 NE 25th Avenue, Portland, OR, 97232