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“Lutronic” Clarity II LPA Laser System - Taiwan Registration 2c76cee9744230b76fab9c2e4f47ec68

Access comprehensive regulatory information for “Lutronic” Clarity II LPA 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 2c76cee9744230b76fab9c2e4f47ec68 and manufactured by Lutronic Corporation. The authorized representative in Taiwan is TBMS INTERNATIONAL CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2c76cee9744230b76fab9c2e4f47ec68
Registration Details
Taiwan FDA Registration: 2c76cee9744230b76fab9c2e4f47ec68
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Device Details

“Lutronic” Clarity II LPA Laser System
TW: “露旎可”克萊媞II雷射系統
Risk Class 2
MD

Registration Details

2c76cee9744230b76fab9c2e4f47ec68

Ministry of Health Medical Device Import No. 035297

DHA05603529706

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Mar 15, 2022

Mar 15, 2027