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“Cynosure” Cellulaze Laser System - Taiwan Registration 4f2cc1ad6eb479641062e38a64978b0e

Access comprehensive regulatory information for “Cynosure” Cellulaze 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 4f2cc1ad6eb479641062e38a64978b0e and manufactured by CYNOSURE, LLC. The authorized representative in Taiwan is QUALTECH CONSULTING 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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4f2cc1ad6eb479641062e38a64978b0e
Registration Details
Taiwan FDA Registration: 4f2cc1ad6eb479641062e38a64978b0e
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Device Details

“Cynosure” Cellulaze Laser System
TW: “色若修”色露蕾絲雷射儀
Risk Class 2
MD

Registration Details

4f2cc1ad6eb479641062e38a64978b0e

Ministry of Health Medical Device Import No. 025349

DHA05602534906

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Jan 22, 2014

Jan 22, 2024