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Speculum, vaginal, single use - ARTG 355592

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 registered under ARTG number 355592 and 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.

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TGA ARTG Official Data
Class Is
ARTG 355592
Class Is
Speculum, vaginal, single use
ARTG ID: 355592
Good Name: Wishmed Pty Ltd - Speculum, vaginal, single use
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Intended Purpose

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.

Device Classification
Risk Class
Class Is
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
355592
Start Date
February 25, 2021
Effective Date
February 25, 2021
Sponsor
Manufacturer
Country
China
Address
Room 601 Unit 1 Building 19 Zhedong Leisure Home Furnishing City, Datian Street Linhai Taizhou, Zhejiang Province, 317004