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"Kentila" Alexander Laser - Taiwan Registration fea860eff7a12e57b5aa52fb628f1a54

Access comprehensive regulatory information for "Kentila" Alexander Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fea860eff7a12e57b5aa52fb628f1a54 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES 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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fea860eff7a12e57b5aa52fb628f1a54
Registration Details
Taiwan FDA Registration: fea860eff7a12e57b5aa52fb628f1a54
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Device Details

"Kentila" Alexander Laser
TW: "่‚ฏ็ฌฌๆ‹‰ "ไบžๆญทๅฑฑๅคง้›ทๅฐ„
Risk Class 2
Cancelled

Registration Details

fea860eff7a12e57b5aa52fb628f1a54

DHA00600922006

Company Information

United States

Product Details

2199 Other medical laser devices

import

Dates and Status

Jun 28, 1999

Nov 04, 2016

May 25, 2018

Cancellation Information

Logged out

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