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"Wonderrhenium" light source system - Taiwan Registration 72839e0986cd29ed80ae820579db59dc

Access comprehensive regulatory information for "Wonderrhenium" light source system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72839e0986cd29ed80ae820579db59dc and manufactured by BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory. The authorized representative in Taiwan is Guangyan Biomedical Technology 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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Registration Details
Taiwan FDA Registration: 72839e0986cd29ed80ae820579db59dc
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Device Details

"Wonderrhenium" light source system
TW: โ€œๆ—บๅพท้Œธโ€ๅ…‰ๆบ็ณป็ตฑ
Risk Class 2

Registration Details

72839e0986cd29ed80ae820579db59dc

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Contract manufacturing;; Domestic

Dates and Status

Jul 04, 2022

Jul 04, 2027