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e.p.t.q. Lidocaine S100 - Synthetic-fluid tissue reconstructive material, anaesthetic - ARTG 441993

Access comprehensive regulatory information for e.p.t.q. Lidocaine S100 - Synthetic-fluid tissue reconstructive material, anaesthetic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 441993 and sponsored by Xytide Biotech Pty Ltd, manufactured by Jetema Co Ltd in South Korea. The device registration started on February 22, 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 III
ARTG 441993
Class III
e.p.t.q. Lidocaine S100 - Synthetic-fluid tissue reconstructive material, anaesthetic
ARTG ID: 441993
Good Name: Xytide Biotech Pty Ltd - e.p.t.q. Lidocaine S100 - Synthetic-fluid tissue reconstructive material, anaesthetic
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Intended Purpose

e.p.t.q. Lidocaine (S100) is intended to be used for the correction of nasolabial folds. The product is for cosmetic use only. The addition of lidocaine provides a pain-relieving effect during treatment.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
441993
Start Date
February 22, 2024
Effective Date
February 22, 2024
Manufacturer
Country
South Korea
Address
16-25 Dongbaekjungang-ro 16beon-gil Giheung-gu, Yongin-si, Gyeonggi-do