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ECHELON ENDOPATH™ Staple Line Reinforcement - Mesh, polymeric, biodegradable - ARTG 448305

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 registered under ARTG number 448305 and 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.

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Class III
ARTG 448305
Class III
ECHELON ENDOPATH™ Staple Line Reinforcement - Mesh, polymeric, biodegradable
ARTG ID: 448305
Good Name: Johnson & Johnson Medical Pty Ltd - ECHELON ENDOPATH™ Staple Line Reinforcement - Mesh, polymeric, biodegradable
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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.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
448305
Start Date
May 09, 2024
Effective Date
May 09, 2024
Manufacturer
Country
Puerto Rico
Address
475 Calle C, Guaynabo, 00969