Australia TGA ARTG record

Plugger, endodontic, hand-held

Australia TGA ARTG Registered Device · KIVEXMEDICAL PTY LTD · Mani Inc · Class I · Started October 15, 2021

Good Name: KIVEXMEDICAL PTY LTD - Plugger, endodontic, hand-held

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: October 15, 2021
Effective Date: October 15, 2021

Sponsor

Name: KIVEXMEDICAL PTY LTD

Manufacturer

Name: Mani Inc
Country: Japan
Address: 8-3 Kiyohara Industrial Park, Utsunomiya, Tochigi, 321-3231

Intended purpose

Pluggers are used to condense gutta percha for the final sealing of the canal and dentinal tubules.

About this record

Access comprehensive regulatory information for Plugger, endodontic, hand-held in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by KIVEXMEDICAL PTY LTD, manufactured by Mani Inc in Japan. The device registration started on October 15, 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.