Australia TGA ARTG record

Neutral plasma wound/lesion disinfection system beam source cover

Australia TGA ARTG Registered Device · Cardio-Jenic Pty Ltd · neoplas med GmbH · Class Is · Started November 24, 2022

Good Name: Cardio-Jenic Pty Ltd - Neutral plasma wound/lesion disinfection system beam source cover

Device classification

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

Registration information

Start Date: November 24, 2022
Effective Date: November 24, 2022

Sponsor

Name: Cardio-Jenic Pty Ltd

Manufacturer

Name: neoplas med GmbH
Country: Germany
Address: Walther-Rathenau-Str 49a, Greifswald, 17489

Intended purpose

sterile spacer for application of cold plasma treatment

About this record

Access comprehensive regulatory information for Neutral plasma wound/lesion disinfection system beam source cover in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Is is sponsored by Cardio-Jenic Pty Ltd, manufactured by neoplas med GmbH in Germany. The device registration started on November 24, 2022.

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.