Australia TGA ARTG record

ECHELON ENDOPATH™ Staple Line Reinforcement - Mesh, polymeric, biodegradable

Australia TGA ARTG Registered Device · Johnson & Johnson Medical Pty Ltd · Ethicon Endo Surgery LLC · Class III · Started May 09, 2024

Good Name: Johnson & Johnson Medical Pty Ltd - ECHELON ENDOPATH™ Staple Line Reinforcement - Mesh, polymeric, biodegradable

Device classification

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

Registration information

Start Date: May 09, 2024
Effective Date: May 09, 2024

Sponsor

Name: Johnson & Johnson Medical Pty Ltd

Manufacturer

Name: Ethicon Endo Surgery LLC
Country: Puerto Rico
Address: 475 Calle C, Guaynabo, 00969

Intended purpose

ECHELON ENDOPATH™ Staple Line Reinforcement is indicated for use in surgical procedures in which soft tissue transection or resection with staple line reinforcement is desired. ECHELON ENDOPATH™ Staple Line Reinforcement can be used for reinforcement of staple lines during lung parenchyma and gastrointestinal procedures.

About this record

Access comprehensive regulatory information for ECHELON ENDOPATH™ Staple Line Reinforcement - Mesh, polymeric, biodegradable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Johnson & Johnson Medical Pty Ltd, manufactured by Ethicon Endo Surgery LLC in Puerto Rico. The device registration started on May 09, 2024.

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.