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“DEKA” SMARTXIDE2 LASER SYSTEM - Taiwan Registration 315efd4045e6a71a8f700634644fad6b

Access comprehensive regulatory information for “DEKA” SMARTXIDE2 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 315efd4045e6a71a8f700634644fad6b and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA 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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315efd4045e6a71a8f700634644fad6b
Registration Details
Taiwan FDA Registration: 315efd4045e6a71a8f700634644fad6b
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Device Details

“DEKA” SMARTXIDE2 LASER SYSTEM
TW: “德卡”絲瑪雷射系統
Risk Class 2
MD

Registration Details

315efd4045e6a71a8f700634644fad6b

Ministry of Health Medical Device Import No. 026356

DHA05602635608

Company Information

Italy

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

Jul 28, 2014

Jul 28, 2024