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Clamp, surgical, tubing, single use - ARTG 459238

Access comprehensive regulatory information for Clamp, surgical, tubing, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 459238 and sponsored by Fresenius Kabi Australia Pty Ltd, manufactured by Fresenius Kabi AG in Germany. The device registration started on August 12, 2024.

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 459238
Class I
Clamp, surgical, tubing, single use
ARTG ID: 459238
Good Name: Fresenius Kabi Australia Pty Ltd - Clamp, surgical, tubing, single use
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Intended Purpose

A tube clamp used with PEG (Percutaneous Endoscopic Gastrostomy) tubes, designed to prevent leakage from the feeding tube when the cap at the end of the tube is opened or closed during feeds, flushing, or medication delivery.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
459238
Start Date
August 12, 2024
Effective Date
August 12, 2024
Manufacturer
Country
Germany
Address
Else-Krรถner-strasse 1, Bad Homburg, D-61352