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Surgical staple remover, single-use - ARTG 408591

Access comprehensive regulatory information for Surgical staple remover, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 408591 and sponsored by Johnson & Johnson Medical Pty Ltd, manufactured by Ethicon Endo Surgery LLC in Puerto Rico. The device registration started on May 08, 2023.

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 IIa
ARTG 408591
Class IIa
Surgical staple remover, single-use
ARTG ID: 408591
Good Name: Johnson & Johnson Medical Pty Ltd - Surgical staple remover, single-use
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Intended Purpose

A sterile single use surgical instrument intended to be used to remove skin staples after the healing process has progressed sufficiently to permit the borders of the wound or incision to remain together without assistance.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
408591
Start Date
May 08, 2023
Effective Date
May 08, 2023
Manufacturer
Country
Puerto Rico
Address
475 Calle C, Guaynabo, 00969