Australia TGA ARTG record

Electrosurgical diathermy system cable, single-use

Australia TGA ARTG Registered Device · CK Surgitech Pty Ltd · Creo Medical Limited · Class I · Started November 16, 2018

Good Name: CK Surgitech Pty Ltd - Electrosurgical diathermy system cable, single-use

Device classification

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

Registration information

Start Date: November 16, 2018
Effective Date: November 16, 2018

Sponsor

Name: CK Surgitech Pty Ltd

Manufacturer

Name: Creo Medical Limited
Country: United Kingdom
Address: Creo House Unit 2 Beaufort Park, Beaufort Park Way, Chepstow, NP165UH

Intended purpose

The Interface Cable is for connection only of a compatible Creo Medical instrument (surgical accessory) to the Creo Medical electrosurgical generator to deliver Radiofrequency (RF) and Microwave Energy for the cutting, coagulation, and ablation of tissue.

About this record

Access comprehensive regulatory information for Electrosurgical diathermy system cable, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by CK Surgitech Pty Ltd, manufactured by Creo Medical Limited in United Kingdom. The device registration started on November 16, 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.