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saypha volume Plus Lidocaine - Synthetic-fluid tissue reconstructive material, anaesthetic - ARTG 475368

Access comprehensive regulatory information for saypha volume Plus Lidocaine - 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 475368 and sponsored by AA-Med Pty Ltd, manufactured by Croma-Pharma GmbH in Austria. The device registration started on January 08, 2025.

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 475368
Class III
saypha volume Plus Lidocaine - Synthetic-fluid tissue reconstructive material, anaesthetic
ARTG ID: 475368
Good Name: AA-Med Pty Ltd - saypha volume Plus Lidocaine - Synthetic-fluid tissue reconstructive material, anaesthetic
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Intended Purpose

The intended aesthetic purpose of saypha volume Plus Lidocaine the device is to restore facial volume. It is indicated to correct moderate to severe midface volume defecit. It must be administered by deep subcutaneous and/or supraperiosteal injection.

Device Classification
Risk Class
Class III
Product Type
Procedure Pack
ARTG Category
General
Registration Information
ARTG ID
475368
Start Date
January 08, 2025
Effective Date
January 08, 2025
Sponsor
Manufacturer
Country
Austria
Address
Industriezeile 6, Leobendorf, 2100