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Q Switch laser system - Dermatological Nd:YAG laser system

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 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.

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Class IIb
Class IIb
Q Switch laser system - Dermatological Nd:YAG laser system
Australia TGA ARTG Registered Device
Good Name: Device Consulting Pty Ltd - Q Switch laser system - Dermatological Nd:YAG laser system
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Intended Purpose

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, Beckerยดs nevus, Benign pigmentation, Cafรจ au lait, Dyschromia, Hori`s macules, Lentigines, Melasma, Nevus Ota, Nevus spilus, Permanent Make-up, Pigmented Lesions, Scars/Acne, Striae, Tattoo, Wrinkles.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
March 06, 2020
Effective Date
March 06, 2020
Manufacturer
Country
Germany
Address
Brusseler Strasse 10, Jena, 07747