Pure Global

Juvederm VOLUX - Synthetic-fluid tissue reconstructive material, anaesthetic

Access comprehensive regulatory information for Juvederm VOLUX - 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 sponsored by Abbvie Pty Ltd, manufactured by Allergan in France. The device registration started on December 10, 2019.

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class III
Class III
Juvederm VOLUX - Synthetic-fluid tissue reconstructive material, anaesthetic
Australia TGA ARTG Registered Device
Good Name: Abbvie Pty Ltd - Juvederm VOLUX - Synthetic-fluid tissue reconstructive material, anaesthetic
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

Juvรฉdermยฎ VOLUXโ„ข is an injectable implant intended to restore and create volume of the face. The presence of lidocaine is meant to reduce the patientโ€™s pain during treatment.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 10, 2019
Effective Date
December 10, 2019
Sponsor
Manufacturer
Country
France
Address
Route de Promery , Zone Artisanale de Pre Mairy, Pringy, Annecy, 74370