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"Denona" skin laser - Taiwan Registration a6949998fbe7544adacb4e53ad860288

Access comprehensive regulatory information for "Denona" skin laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a6949998fbe7544adacb4e53ad860288 and manufactured by DINONA INC.. The authorized representative in Taiwan is COLLAMATRIX 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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a6949998fbe7544adacb4e53ad860288
Registration Details
Taiwan FDA Registration: a6949998fbe7544adacb4e53ad860288
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Device Details

"Denona" skin laser
TW: โ€œ้ป›่ซพๅจœโ€็šฎ่†š้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

a6949998fbe7544adacb4e53ad860288

DHA00601875303

Company Information

Korea, Republic of

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

Mar 28, 2008

Mar 28, 2018

Nov 15, 2019

Cancellation Information

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