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Steam sterilization indication system - ARTG 389991

Access comprehensive regulatory information for Steam sterilization indication system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 389991 and sponsored by KCI Medical Australia Pty Ltd, manufactured by 3M Deutschland GmbH in Germany. The device registration started on June 10, 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.

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TGA ARTG Official Data
Class I
ARTG 389991
Class I
Steam sterilization indication system
ARTG ID: 389991
Good Name: KCI Medical Australia Pty Ltd - Steam sterilization indication system
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Intended Purpose

The primary function of the device is to monitor the air removal stage and the sterilization phase of a steam sterilization cycle.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
389991
Start Date
June 10, 2022
Effective Date
June 10, 2022
Manufacturer
Country
Germany
Address
Carl-Schurz-Strasse 1, Neuss, 41453