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Speculum, vaginal, single use - ARTG 473025

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 I is registered under ARTG number 473025 and sponsored by YES Medical, manufactured by Taizhou Honod Medical Co Ltd in China. The device registration started on December 13, 2024.

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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Class I
ARTG 473025
Class I
Speculum, vaginal, single use
ARTG ID: 473025
Good Name: YES Medical - Speculum, vaginal, single use
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Intended Purpose

Speculum with in-built LED light for viewing the vagina and cervix, for diagnostic purposes.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
473025
Start Date
December 13, 2024
Effective Date
December 13, 2024
Sponsor
Manufacturer
Country
China
Address
Room 601 Unit 1 Building 19 Zhedong Leisure Home Furnishing City, Datian Street Linhai Taizhou, Zhejiang Province, 317004