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Non-implantable needle guide, single-use

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.

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TGA ARTG Official Data
Class Is
Class Is
Non-implantable needle guide, single-use
Australia TGA ARTG Registered Device
Good Name: Bosco Medical Australia - Non-implantable needle guide, single-use
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Intended Purpose

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.

Device Classification
Risk Class
Class Is
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 20, 2018
Effective Date
February 20, 2018
Manufacturer
Country
United Kingdom
Address
300 City Gate London Road, Derby, DE248WY