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Electrosurgical diathermy system cable, single-use

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.

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TGA ARTG Official Data
Class I
Class I
Electrosurgical diathermy system cable, single-use
Australia TGA ARTG Registered Device
Good Name: CK Surgitech Pty Ltd - Electrosurgical diathermy system cable, single-use
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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.

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
Manufacturer
Country
United Kingdom
Address
Creo House Unit 2 Beaufort Park, Beaufort Park Way, Chepstow, NP165UH