Australia TGA ARTG record

Foetal vacuum extraction cup, single-use

Australia TGA ARTG Registered Device · Endotherapeutics Pty Ltd · Cooper Surgical Inc · Class IIa · Started September 11, 2018

Good Name: Endotherapeutics Pty Ltd - Foetal vacuum extraction cup, single-use

Device classification

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

Registration information

Start Date: September 11, 2018
Effective Date: September 11, 2018

Sponsor

Name: Endotherapeutics Pty Ltd

Manufacturer

Name: Cooper Surgical Inc
Country: United States of America
Address: 95 Corporate Drive, Trumbull, CT, 06611

Intended purpose

A single use extraction cup intended to be used in conjunction with an electrical vacuum source to assist in the delivery of a foetus.

About this record

Access comprehensive regulatory information for Foetal vacuum extraction cup, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Endotherapeutics Pty Ltd, manufactured by Cooper Surgical Inc in United States of America. The device registration started on September 11, 2018.

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.