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"Kentila" pulsed dye laser system - Taiwan Registration 3b5e2f0b88505de61b3d1210c06cfffb

Access comprehensive regulatory information for "Kentila" pulsed dye laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b5e2f0b88505de61b3d1210c06cfffb and manufactured by Valtronic Technologies (Suisse) SA;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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3b5e2f0b88505de61b3d1210c06cfffb
Registration Details
Taiwan FDA Registration: 3b5e2f0b88505de61b3d1210c06cfffb
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Device Details

"Kentila" pulsed dye laser system
TW: "่‚ฏ็ฌฌๆ‹‰"่„ˆ่กๆŸ“ๆ–™้›ทๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

3b5e2f0b88505de61b3d1210c06cfffb

DHA00601672909

Company Information

United States;;Switzerland

Product Details

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

I General, Plastic Surgery and Dermatology

Input;; Contract manufacturing

Dates and Status

Jun 23, 2006

Jun 23, 2026