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“Fotona” Dynamis Line Laser System - Taiwan Registration de8f574740a29bd1dd8ba8bb9c506fd2

Access comprehensive regulatory information for “Fotona” Dynamis Line 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 de8f574740a29bd1dd8ba8bb9c506fd2 and manufactured by Fotona d.o.o.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES 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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de8f574740a29bd1dd8ba8bb9c506fd2
Registration Details
Taiwan FDA Registration: de8f574740a29bd1dd8ba8bb9c506fd2
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Device Details

“Fotona” Dynamis Line Laser System
TW: “富多拿”黛娜美斯雅各多功能雷射系統
Risk Class 2
MD

Registration Details

de8f574740a29bd1dd8ba8bb9c506fd2

Ministry of Health Medical Device Import No. 028367

DHA05602836700

Company Information

Slovenia

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

Apr 12, 2016

Apr 12, 2021