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“SCITON” mJoule System - Taiwan Registration 9402fb8c8902df16e295564d015e0534

Access comprehensive regulatory information for “SCITON” mJoule System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9402fb8c8902df16e295564d015e0534 and manufactured by SCITON, INC.. The authorized representative in Taiwan is WOH MEDICAL 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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9402fb8c8902df16e295564d015e0534
Registration Details
Taiwan FDA Registration: 9402fb8c8902df16e295564d015e0534
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Device Details

“SCITON” mJoule System
TW: “西頓”迷你吉爾寬頻光照及雷射系統
Risk Class 2
MD

Registration Details

9402fb8c8902df16e295564d015e0534

Ministry of Health Medical Device Import No. 035731

DHA05603573109

Company Information

United States

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

Aug 03, 2022

Aug 03, 2027