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"Quantel" diode laser system - Taiwan Registration e9f2f4285ce5915266c98d17d15b7503

Access comprehensive regulatory information for "Quantel" diode 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 e9f2f4285ce5915266c98d17d15b7503 and manufactured by QUANTEL DERMA GMBH. The authorized representative in Taiwan is Dongzhe Riki Medical Co., Ltd.

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e9f2f4285ce5915266c98d17d15b7503
Registration Details
Taiwan FDA Registration: e9f2f4285ce5915266c98d17d15b7503
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Device Details

"Quantel" diode laser system
TW: โ€œๅฏฌ็‰น็ˆพโ€ไบŒๆฅต้ซ”้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e9f2f4285ce5915266c98d17d15b7503

DHA00602262509

Company Information

Germany

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

Aug 04, 2011

Aug 04, 2016

Feb 21, 2018

Cancellation Information

Logged out

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