“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.
Device Details
Registration Details
55ab3b4851adb6d780543dd08a5f4f23
Ministry of Health Medical Device Import No. 029053
DHA05602905305
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

