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"Denona" diode laser - Taiwan Registration fbbf971a938e6faf03f5e1ca1ac29b79

Access comprehensive regulatory information for "Denona" diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fbbf971a938e6faf03f5e1ca1ac29b79 and manufactured by DINONA INC.. The authorized representative in Taiwan is Dongzhe Riki Medical Co., Ltd.

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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fbbf971a938e6faf03f5e1ca1ac29b79
Registration Details
Taiwan FDA Registration: fbbf971a938e6faf03f5e1ca1ac29b79
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Device Details

"Denona" diode laser
TW: โ€œ้ป›่ซพๅจœโ€ไบŒๆฅต้ซ”้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

fbbf971a938e6faf03f5e1ca1ac29b79

DHA00601977403

Company Information

Korea, Republic of

Product Details

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

I General, Plastic Surgery and Dermatology

import

Dates and Status

Apr 13, 2009

Apr 13, 2014

Jan 09, 2017

Cancellation Information

Logged out

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