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“Candela” Profound Matrix System - Taiwan Registration 3e627f8d35b19a424d5102e5db9b449b

Access comprehensive regulatory information for “Candela” Profound Matrix System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e627f8d35b19a424d5102e5db9b449b and manufactured by Candela Corporation;;NPA DE MEXICO, S. DE R.L. DE C.V.. The authorized representative in Taiwan is Taike Medical Technology Co.,Ltd.

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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3e627f8d35b19a424d5102e5db9b449b
Registration Details
Taiwan FDA Registration: 3e627f8d35b19a424d5102e5db9b449b
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Device Details

“Candela” Profound Matrix System
TW: “坎德拉”波芳美萃煥膚除皺系統
Risk Class 2
MD

Registration Details

3e627f8d35b19a424d5102e5db9b449b

Ministry of Health Medical Device Import No. 036710

DHA05603671006

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I0001 High Density Energy Current Wrinkle Remover

Imported from abroad; Contract manufacturing

Dates and Status

Aug 29, 2023

Aug 29, 2028