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Sterilization packaging, reusable - ARTG 392397

Access comprehensive regulatory information for Sterilization packaging, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 392397 and sponsored by Endogear Pty Ltd, manufactured by Kohdent Roland Kohler Medizinetechnik GmbH & Co KG in Germany. The device registration started on July 18, 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 392397
Class I
Sterilization packaging, reusable
ARTG ID: 392397
Good Name: Endogear Pty Ltd - Sterilization packaging, reusable
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Intended Purpose

It is designed to allow sterilzation of he enclosed medical device and also to maintain sterility of the device until the packaging is opened for use of the device.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
392397
Start Date
July 18, 2022
Effective Date
July 18, 2022
Sponsor
Manufacturer
Country
Germany
Address
Bodenseealle 14-16, Stockach, 78333