Australia TGA ARTG recordCatheter tunneller single use
Australia TGA ARTG Registered Device · Teleflex Medical Australia Pty Ltd · Ace Medical Co Ltd · Class IIa · Started August 14, 2020
Good Name: Teleflex Medical Australia Pty Ltd - Catheter tunneller single use
- Risk Class
- Class IIa
- Product Type
- Medical device system
- ARTG Category
- General
- Start Date
- August 14, 2020
- Effective Date
- August 14, 2020
- Country
- South Korea
- Address
- 33 Naeyoo-Road 124 Deogyang-Gu Goyang-Si, Gyeonggi-Do
Tunneler is a sterile, single-use device indicated for use in the percutaneous introduction of catheters into and around the surgical wound site or close to the nerve. It is intended for transient use.
Access comprehensive regulatory information for Catheter tunneller single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Teleflex Medical Australia Pty Ltd, manufactured by Ace Medical Co Ltd in South Korea. The device registration started on August 14, 2020.
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.