Pure Global

Dental implant suprastructure device, temporary, reusable

Access comprehensive regulatory information for Dental implant suprastructure device, temporary, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Neoss Australia Pty Ltd, manufactured by Elos Medtech Pinol A/S in Denmark. The device registration started on January 20, 2021.

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 I
Class I
Dental implant suprastructure device, temporary, reusable
Australia TGA ARTG Registered Device
Good Name: Neoss Australia Pty Ltd - Dental implant suprastructure device, temporary, reusable
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Intended Purpose

The Scan Body is intended to be used together with a dental scanner to locate the exact position of an implant/analog or abutment in relation to prosthetic restorations. The scan body is intended to be mounted directly on the implant/analog or abutment using the Scan Body Driver/Neo Screwdriver. The Scan Body is intended to be used directly in a patientโ€™s mouth when using an Intra oral scanner, or on a model of the patientsโ€™ teeth setup when using a desktop scanner

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
January 20, 2021
Effective Date
January 20, 2021
Manufacturer
Country
Denmark
Address
Engvej 33, Gorlose, 3330