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Endoscopic insufflation tubing set - ARTG 463508

Access comprehensive regulatory information for Endoscopic insufflation tubing set in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 463508 and sponsored by Compliance Management Solutions, manufactured by GRI Medical & Electronic Technology Co Ltd in China. The device registration started on October 02, 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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Class IIa
ARTG 463508
Class IIa
Endoscopic insufflation tubing set
ARTG ID: 463508
Good Name: Compliance Management Solutions - Endoscopic insufflation tubing set
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Intended Purpose

Insufflation Tubing is intended to provide a filtered connection between the insufflation equipment and the Veress Needle or Trocar to provide the gas used to establish the pneumoperitoneum in the patient for the purposes of certain minimally invasive surgical procedures. This device is supplied in sterile and non-sterile form and is for single use only.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
463508
Start Date
October 02, 2024
Effective Date
October 02, 2024
Manufacturer
Country
China
Address
1805 Honggao Road, Jiaxing, Zhejiang, 314031