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“Dornier” Thulio Performance Fiber - Taiwan Registration 7e8b21cb5678fe1b44b762c79884c966

Access comprehensive regulatory information for “Dornier” Thulio Performance Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e8b21cb5678fe1b44b762c79884c966 and manufactured by Dornier MedTech America, Inc.. The authorized representative in Taiwan is MEDEN INTERNATIONAL 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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7e8b21cb5678fe1b44b762c79884c966
Registration Details
Taiwan FDA Registration: 7e8b21cb5678fe1b44b762c79884c966
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Device Details

“Dornier” Thulio Performance Fiber
TW: “多尼爾”舒立歐效能光纖
Risk Class 2
MD

Registration Details

7e8b21cb5678fe1b44b762c79884c966

Ministry of Health Medical Device Import No. 036663

DHA05603666300

Company Information

United States

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

Jul 05, 2023

Jul 05, 2028