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Process Challenge Device - Sterilization process indicator, <specify>

Access comprehensive regulatory information for Process Challenge Device - Sterilization process indicator, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by National Compliance Australia, manufactured by Verify Dental UK in United Kingdom. The device registration started on June 15, 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
Process Challenge Device - Sterilization process indicator, <specify>
Australia TGA ARTG Registered Device
Good Name: National Compliance Australia - Process Challenge Device - Sterilization process indicator, <specify>
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Intended Purpose

NCA Verify+ Brass Helix is used as a process challenge device to monitor the presence of non-condensible gases in the sterilising chamber and cannulated instruments

Device Classification
Risk Class
Class I
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
June 15, 2018
Effective Date
June 15, 2018
Sponsor
Manufacturer
Country
United Kingdom
Address
Lagonda Road Cowpen Industrial Estate, Billingham, Teesside