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Cuff, tourniquet, reusable - ARTG 458487

Access comprehensive regulatory information for Cuff, tourniquet, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 458487 and sponsored by Bosco Medical Australia, manufactured by Vbm Medizintechnik GmbH in Germany. The device registration started on August 05, 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 458487
Class I
Cuff, tourniquet, reusable
ARTG ID: 458487
Good Name: Bosco Medical Australia - Cuff, tourniquet, reusable
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Intended Purpose

A bandlike cuff device for reusable purposes to assist in temporarily occluding the blood flow to in create and maintain a bloodless field during theatre procedures to the patient's extremity (arm or leg).

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
458487
Start Date
August 05, 2024
Effective Date
August 05, 2024
Manufacturer
Country
Germany
Address
Einsteinstr 1, Sulz a N, 72172