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Haematological concentrate system kit, platelet concentration

ARTG ID: 332264 · Ebos Medical Devices Australia Pty Ltd · T-Biyoteknoloji Laboratuvar Estetik Medikal Kozmetik San Ve Tic LTD STI · Class IIb · Started March 24, 2020

Good Name: Ebos Medical Devices Australia Pty Ltd - Haematological concentrate system kit, platelet concentration

Device classification
Risk Class
Class IIb
Product Type
Procedure Pack
ARTG Category
General
Registration information
ARTG ID
332264
Start Date
March 24, 2020
Effective Date
March 24, 2020
Sponsor
Manufacturer
Country
Turkey
Address
Tahtali Mah Degirmen Yolu Sk No 10 Nilufer, Bursa, 460
Intended purpose

The system is designed to be used for the preparation of autologous platelet-rich-plasma (PRP) from a small sample of blood at the patient's point of care. The PRP is prepared prior to the application to a local area of soft or hard tissue (including bone) site as deemed necessary by the clinical use requirements.

About this record

Access comprehensive regulatory information for Haematological concentrate system kit, platelet concentration in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 332264 and sponsored by Ebos Medical Devices Australia Pty Ltd, manufactured by T-Biyoteknoloji Laboratuvar Estetik Medikal Kozmetik San Ve Tic LTD STI in Turkey. The device registration started on March 24, 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.

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