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“Dornier” Thulio Laser Device - Taiwan Registration 16efecdeb18faa0aff14c0d9e71f3a95

Access comprehensive regulatory information for “Dornier” Thulio Laser Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16efecdeb18faa0aff14c0d9e71f3a95 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. 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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16efecdeb18faa0aff14c0d9e71f3a95
Registration Details
Taiwan FDA Registration: 16efecdeb18faa0aff14c0d9e71f3a95
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Device Details

“Dornier” Thulio Laser Device
TW: “多尼爾”舒立歐雷射
Risk Class 2
MD

Registration Details

16efecdeb18faa0aff14c0d9e71f3a95

Ministry of Health Medical Device Import No. 036660

DHA05603666004

Company Information

Germany

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 03, 2023

Jul 03, 2028