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"Daxin" pulsed light system - Taiwan Registration 11dbfc1fe134a4af2007a87821574c33

Access comprehensive regulatory information for "Daxin" pulsed light system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11dbfc1fe134a4af2007a87821574c33 and manufactured by DAESHIN ENTERPRISE. The authorized representative in Taiwan is PIEZOMED 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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11dbfc1fe134a4af2007a87821574c33
Registration Details
Taiwan FDA Registration: 11dbfc1fe134a4af2007a87821574c33
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Device Details

"Daxin" pulsed light system
TW: โ€œๅคงๆ–ฐโ€่„ˆ่กๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

11dbfc1fe134a4af2007a87821574c33

DHA00601854509

Company Information

Korea, Republic of

Product Details

Treatment of pigmented lesions, vascular lesions, and hair removal.

I General, Plastic Surgery and Dermatology

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

import

Dates and Status

Jan 16, 2008

Jan 16, 2018

Nov 20, 2019

Cancellation Information

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