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Dilator, oesophageal

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.

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TGA ARTG Official Data
Class IIa
Class IIa
Dilator, oesophageal
Australia TGA ARTG Registered Device
Good Name: CK Surgitech Pty Ltd - Dilator, oesophageal
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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.

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
Manufacturer
Country
China
Address
2 floor of 6 Building Langshan Industry Park No 30 Zilang Road, Nantong City, Jiangsu, 226000