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HOLLYWOOD SPECTRA - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system

Access comprehensive regulatory information for HOLLYWOOD SPECTRA - Dermatological Nd:YAG/frequency-doubled 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 Ebos Medical Devices Australia Pty Ltd, manufactured by Lutronic Corporation in South Korea. The device registration started on October 20, 2023.

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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TGA ARTG Official Data
Class IIb
Class IIb
HOLLYWOOD SPECTRA - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
Australia TGA ARTG Registered Device
Good Name: Ebos Medical Devices Australia Pty Ltd - HOLLYWOOD SPECTRA - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
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Intended Purpose

HOLLYWOOD SPECTRA is a medical device laser system that is indicated for use in surgical applications requiring the ablation, removal, incision, and destruction of soft tissue in medical specialities. The device is indicated for epidermal pigmented lesions, epidermal & dermal pigmented lesions, dermal pigmented lesions, facial telangiectasia, scars.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
October 20, 2023
Effective Date
October 20, 2023
Manufacturer
Country
South Korea
Address
Lutronic Center 219 Sowon-ro Deogyang-gu, Goyang-si, Gyeonggi-do