Australia TGA ARTG recordSpeculum, vaginal, single use
Australia TGA ARTG Registered Device · Wishmed Pty Ltd · Taizhou Honod Medical Co Ltd · Class Is · Started February 25, 2021
Good Name: Wishmed Pty Ltd - Speculum, vaginal, single use
- Risk Class
- Class Is
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- February 25, 2021
- Effective Date
- February 25, 2021
- Name
- Wishmed Pty Ltd
- Country
- China
- Address
- Room 601 Unit 1 Building 19 Zhedong Leisure Home Furnishing City, Datian Street Linhai Taizhou, Zhejiang Province, 317004
Vaginal Speculum is used during examination and treatment of the vagina to provide access to the interior, usually by expanding/distending the opening to this orifice. This device may be designed with adjustable or fixed blades and may have built-in lighting. The device is made of plastic and is single-use and sterile.
Access comprehensive regulatory information for Speculum, vaginal, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Is is sponsored by Wishmed Pty Ltd, manufactured by Taizhou Honod Medical Co Ltd in China. The device registration started on February 25, 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.