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“EUFOTON” LASEmaR mini Diode Laser System - Taiwan Registration 8211c90c4203a680b033fffff69d6ab4

Access comprehensive regulatory information for “EUFOTON” LASEmaR mini Diode 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 8211c90c4203a680b033fffff69d6ab4 and manufactured by EUFOTON S.R.L.. The authorized representative in Taiwan is Glory Group 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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8211c90c4203a680b033fffff69d6ab4
Registration Details
Taiwan FDA Registration: 8211c90c4203a680b033fffff69d6ab4
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Device Details

“EUFOTON” LASEmaR mini Diode Laser System
TW: “悠扶盾”二極體雷射儀
Risk Class 2
MD

Registration Details

8211c90c4203a680b033fffff69d6ab4

Ministry of Health Medical Device Import No. 036546

DHA05603654606

Company Information

Italy

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

Jun 19, 2023

Jun 19, 2028