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NanoBone Granulate - Bone matrix implant, synthetic - ARTG 281303

Access comprehensive regulatory information for NanoBone Granulate - Bone matrix implant, synthetic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 281303 and sponsored by Emergo Asia Pacific Pty Ltd T/a Emergo Australia, manufactured by Artoss GmbH in Germany. The device registration started on October 12, 2016.

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
ARTG 281303
Class III
NanoBone Granulate - Bone matrix implant, synthetic
ARTG ID: 281303
Good Name: Emergo Asia Pacific Pty Ltd T/a Emergo Australia - NanoBone Granulate - Bone matrix implant, synthetic
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Intended Purpose

NanoBone Granulate is a bone void filler material that is intended to be used for orthopaedic applications as a filler for gaps and voids that are not intrinsic to the stability of the bony structure. It is a sterile bioabsorbable device made of synthetic material intended to be implanted into the body and is provided in granulate form of various sizes.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
281303
Start Date
October 12, 2016
Effective Date
October 12, 2016
Manufacturer
Country
Germany
Address
Fischerweg 421, Rostock, 18069