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REJURAN i - Dermal tissue reconstructive material, animal-derived - ARTG 412631

Access comprehensive regulatory information for REJURAN i - Dermal tissue reconstructive material, animal-derived in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 412631 and sponsored by K Bridge Medical Pty Ltd, manufactured by PharmaResearch Co Ltd in South Korea. The device registration started on July 05, 2023.

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 III
ARTG 412631
Class III
REJURAN i - Dermal tissue reconstructive material, animal-derived
ARTG ID: 412631
Good Name: K Bridge Medical Pty Ltd - REJURAN i - Dermal tissue reconstructive material, animal-derived
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Intended Purpose

REJURAN i, is an injectable gel intended for injection into the mid to deep dermis to promote tissue restoration and reconstruction, and improvement of physical appearance. It is highly versatile and easy to handle and can be used on areas of the face (especially around the eyes, perioral area).

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
412631
Start Date
July 05, 2023
Effective Date
July 05, 2023
Manufacturer
Country
South Korea
Address
77-19 Gwahakdanji-ro Gangneung-si, Gangwon-do, 25452