Australia TGA ARTG record

Dilator, oesophageal

Australia TGA ARTG Registered Device · CK Surgitech Pty Ltd · Jiangsu Ecure Medical Technology Co Ltd · Class IIa · Started December 01, 2020

Good Name: CK Surgitech Pty Ltd - Dilator, oesophageal

Device classification

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

Registration information

Start Date: December 01, 2020
Effective Date: December 01, 2020

Sponsor

Name: CK Surgitech Pty Ltd

Manufacturer

Name: Jiangsu Ecure Medical Technology Co Ltd
Country: China
Address: 2 floor of 6 Building Langshan Industry Park No 30 Zilang Road, Nantong City, Jiangsu, 226000

Intended purpose

A device, typically a surgical instrument, consisting of a slender hollow or solid body made of metal, plastic or other suitable material in a cylindrical form and a variety of sizes and flexibilities that is intended to be used to dilate structures/passages.

About this record

Access comprehensive regulatory information for Dilator, oesophageal in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by CK Surgitech Pty Ltd, manufactured by Jiangsu Ecure Medical Technology Co Ltd in China. The device registration started on December 01, 2020.

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.