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“Lutronic” LaseMD Ultra Thulium Laser System - Taiwan Registration 54209d89c0dd2652a8b81c7c183395f9

Access comprehensive regulatory information for “Lutronic” LaseMD Ultra Thulium Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54209d89c0dd2652a8b81c7c183395f9 and manufactured by Lutronic Corporation. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..

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54209d89c0dd2652a8b81c7c183395f9
Registration Details
Taiwan FDA Registration: 54209d89c0dd2652a8b81c7c183395f9
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Device Details

“Lutronic” LaseMD Ultra Thulium Laser System
TW: “儷妮可”雷絲美奧創銩雷射系統
Risk Class 2
MD

Registration Details

54209d89c0dd2652a8b81c7c183395f9

Ministry of Health Medical Device Import No. 035492

DHA05603549204

Company Information

Korea, Republic of

Product Details

This product is a 19.2nm thulium laser, suitable for wrinkle improvement, dermabrasion and pigment treatment.

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

May 20, 2022

May 20, 2027