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"Denona" CO2 laser - Taiwan Registration 9d15bf5b582421dbc8d80dd474c19830

Access comprehensive regulatory information for "Denona" CO2 laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d15bf5b582421dbc8d80dd474c19830 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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9d15bf5b582421dbc8d80dd474c19830
Registration Details
Taiwan FDA Registration: 9d15bf5b582421dbc8d80dd474c19830
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Device Details

"Denona" CO2 laser
TW: โ€œ้ป›่ซพๅจœโ€ไบŒๆฐงๅŒ–็ขณ้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

9d15bf5b582421dbc8d80dd474c19830

DHA00602086009

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 29, 2010

Mar 29, 2015

Jun 28, 2018

Cancellation Information

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