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"DORNIER" diode laser fiber - Taiwan Registration e587cf74387c41cb15f0681bfed2234c

Access comprehensive regulatory information for "DORNIER" diode 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 e587cf74387c41cb15f0681bfed2234c 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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e587cf74387c41cb15f0681bfed2234c
Registration Details
Taiwan FDA Registration: e587cf74387c41cb15f0681bfed2234c
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Device Details

"DORNIER" diode laser fiber
TW: โ€œๅคšๅฐผ็ˆพโ€ไบŒๆฅต้ซ”้›ทๅฐ„็”จๅ…‰็บ–
Risk Class 2

Registration Details

e587cf74387c41cb15f0681bfed2234c

DHA00602026702

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

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

import

Dates and Status

Oct 27, 2009

Oct 27, 2029