Australia TGA ARTG record

Camera, cine, endoscopic

Australia TGA ARTG Registered Device · Visionflex Pty Ltd · Schoelly Fiberoptic GmbH · Class I · Started July 26, 2017

Good Name: Visionflex Pty Ltd - Camera, cine, endoscopic

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: July 26, 2017
Effective Date: July 26, 2017

Sponsor

Name: Visionflex Pty Ltd

Manufacturer

Name: Schoelly Fiberoptic GmbH
Country: Germany
Address: Robert-Bosch-Strasse 1-3, Denzlingen , 79211

Intended purpose

The FSC2 camera handpiece is used for the visualisation of anatomic structures of the ear, nose throat and dermatological areas.

About this record

Access comprehensive regulatory information for Camera, cine, endoscopic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Visionflex Pty Ltd, manufactured by Schoelly Fiberoptic GmbH in Germany. The device registration started on July 26, 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.