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Speculum, <specify>

Access comprehensive regulatory information for Speculum, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Vorotek Pty Ltd, manufactured by Vorotek Pty Ltd in Australia. The device registration started on November 19, 2019.

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
Speculum, <specify>
Australia TGA ARTG Registered Device
Good Name: Vorotek Pty Ltd - Speculum, <specify>
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Intended Purpose

The Vorotek Speculum range is used to expand or stretch the external ear canal or nasal cavity to facilitate examination.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
November 19, 2019
Effective Date
November 19, 2019
Sponsor
Manufacturer
Country
Australia
Address
23 Point Henry Road, Moolap, VIC, 3224