ARTG 330881Q Switch laser system - Dermatological Nd:YAG laser system
ARTG ID: 330881 · Device Consulting Pty Ltd · Asclepion Laser Technologies GmbH · Class IIb · Started March 06, 2020
Good Name: Device Consulting Pty Ltd - Q Switch laser system - Dermatological Nd:YAG laser system
- Risk Class
- Class IIb
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 330881
- Start Date
- March 06, 2020
- Effective Date
- March 06, 2020
- Country
- Germany
- Address
- Brusseler Strasse 10, Jena, 07747
Vaporization and ablation of soft tissue, particularly for a selective damage of pigments in the epidermis and dermis and thus the gentle treatment of benign pigmented lesions and artificial lesions including Age spots, Aging skin, Becker´s nevus, Benign pigmentation, Cafè au lait, Dyschromia, Hori`s macules, Lentigines, Melasma, Nevus Ota, Nevus spilus, Permanent Make-up, Pigmented Lesions, Scars/Acne, Striae, Tattoo, Wrinkles.
Access comprehensive regulatory information for Q Switch laser system - Dermatological Nd:YAG laser system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 330881 and sponsored by Device Consulting Pty Ltd, manufactured by Asclepion Laser Technologies GmbH in Germany. The device registration started on March 06, 2020.
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.