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“Eufoton” LASEmar Laser - Taiwan Registration 55ab3b4851adb6d780543dd08a5f4f23

Access comprehensive regulatory information for “Eufoton” LASEmar Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55ab3b4851adb6d780543dd08a5f4f23 and manufactured by EUFOTON S.r.l.. The authorized representative in Taiwan is WAY SEEN INTERNATIONAL 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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55ab3b4851adb6d780543dd08a5f4f23
Registration Details
Taiwan FDA Registration: 55ab3b4851adb6d780543dd08a5f4f23
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Device Details

“Eufoton” LASEmar Laser
TW: “優芙登”雷射儀
Risk Class 2
MD
Cancelled

Registration Details

55ab3b4851adb6d780543dd08a5f4f23

Ministry of Health Medical Device Import No. 029053

DHA05602905305

Company Information

Italy

Product Details

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Nov 16, 2016

Nov 16, 2021

Aug 15, 2023

Cancellation Information

Logged out

許可證已逾有效期