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“Dornier” Holmium Laser Fiber - Taiwan Registration 6098250030fea0531e438ab057275706

Access comprehensive regulatory information for “Dornier” Holmium Laser Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6098250030fea0531e438ab057275706 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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6098250030fea0531e438ab057275706
Registration Details
Taiwan FDA Registration: 6098250030fea0531e438ab057275706
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Device Details

“Dornier” Holmium Laser Fiber
TW: “多尼爾”鈥雷射光纖
Risk Class 2
MD

Registration Details

6098250030fea0531e438ab057275706

Ministry of Health Medical Device Import No. 032767

DHA05603276702

Company Information

United States

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

Aug 27, 2019

Aug 27, 2024