ARTG 326349Speculum, <specify>
ARTG ID: 326349 · Vorotek Pty Ltd · Vorotek Pty Ltd · Class I · Started November 19, 2019
Good Name: Vorotek Pty Ltd - Speculum, <specify>
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 326349
- Start Date
- November 19, 2019
- Effective Date
- November 19, 2019
- Name
- Vorotek Pty Ltd
- Name
- Vorotek Pty Ltd
- Country
- Australia
- Address
- 23 Point Henry Road, Moolap, VIC, 3224
The Vorotek Speculum range is used to expand or stretch the external ear canal or nasal cavity to facilitate examination.
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 registered under ARTG number 326349 and 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.