Australia TGA ARTG recordHaematological concentrate system kit, platelet concentration
Australia TGA ARTG Registered Device · 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
- Risk Class
- Class IIb
- Product Type
- Procedure Pack
- ARTG Category
- General
- Start Date
- March 24, 2020
- Effective Date
- March 24, 2020
- Country
- Turkey
- Address
- Tahtali Mah Degirmen Yolu Sk No 10 Nilufer, Bursa, 460
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.
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 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.