Australia TGA ARTG recordNon-implantable needle guide, single-use
Australia TGA ARTG Registered Device · Bosco Medical Australia · Ivor Shaw Limited trading as Pennine Healthcare · Class Is · Started February 20, 2018
Good Name: Bosco Medical Australia - Non-implantable needle guide, single-use
- Risk Class
- Class Is
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- February 20, 2018
- Effective Date
- February 20, 2018
- Country
- United Kingdom
- Address
- 300 City Gate London Road, Derby, DE248WY
Sterile needle guide intended to be used to lead a needle into its proper course when performing a clinical and/or surgical procedure by accurate location of VAPs and subsequent insertion of the Huber needle towards the centre of the port chamber, designed for quick and easy release.
Access comprehensive regulatory information for Non-implantable needle guide, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Is is sponsored by Bosco Medical Australia, manufactured by Ivor Shaw Limited trading as Pennine Healthcare in United Kingdom. The device registration started on February 20, 2018.
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.