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NanoBone SBX Putty - Bone matrix implant, synthetic

Access comprehensive regulatory information for NanoBone SBX Putty - Bone matrix implant, synthetic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Innovative Medcare Technology Pty Ltd, manufactured by Artoss GmbH in Germany. The device registration started on July 31, 2017.

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 III
Class III
NanoBone SBX Putty - Bone matrix implant, synthetic
Australia TGA ARTG Registered Device
Good Name: Innovative Medcare Technology Pty Ltd - NanoBone SBX Putty - Bone matrix implant, synthetic
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Intended Purpose

NanoBone SBX putty is for the reconstruction of bone defects which are not essential for the stability of the bone structure and for augmentation. NanoBone SBX putty can be used for all fields of application for which autologous cancellous bone could be used.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
July 31, 2017
Effective Date
December 05, 2017
Manufacturer
Country
Germany
Address
Fischerweg 421, Rostock, 18069