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Autologous blood collection tube - ARTG 465165

Access comprehensive regulatory information for Autologous blood collection tube in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 465165 and sponsored by Smartfem Pty Ltd, manufactured by T-Biyoteknoloji Laboratuvar Estetik Medikal Kozmetik San Ve Tic LTD STI in Turkey. The device registration started on October 22, 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 465165
Class IIa
Autologous blood collection tube
ARTG ID: 465165
Good Name: Smartfem Pty Ltd - Autologous blood collection tube
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Intended Purpose

The device is designed to be used for the safe and rapid preparation of autologous platelet-rich-plasma (PRP) from a small sample of blood at the patientโ€™s point of care.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
465165
Start Date
October 22, 2024
Effective Date
October 22, 2024
Sponsor
Manufacturer
Country
Turkey
Address
Dumlupฤฑnar mah Kuleli Cad No 3, Nilufer, Bursa