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“CHUNGWOO” CONTLEX HIGH INTENSITY FOCUSED ULTRASOUND (HIFU) - Taiwan Registration 010936d239ce6f45b1a1c532075fa210

Access comprehensive regulatory information for “CHUNGWOO” CONTLEX HIGH INTENSITY FOCUSED ULTRASOUND (HIFU) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 010936d239ce6f45b1a1c532075fa210 and manufactured by Chungwoo Co., Ltd. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..

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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010936d239ce6f45b1a1c532075fa210
Registration Details
Taiwan FDA Registration: 010936d239ce6f45b1a1c532075fa210
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Device Details

“CHUNGWOO” CONTLEX HIGH INTENSITY FOCUSED ULTRASOUND (HIFU)
TW: “青友”康提超音波治療儀
Risk Class 2
MD

Registration Details

010936d239ce6f45b1a1c532075fa210

Ministry of Health Medical Device Import No. 033188

DHA05603318804

Company Information

Korea, Republic of

Product Details

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

I General and plastic surgical devices

I4590 Focused Ultrasound Stimulator

Imported from abroad

Dates and Status

Feb 09, 2020

Feb 09, 2025