"Intermedi" Andu laser diode - Taiwan Registration 0f2a6e429bf99aa4ff96f3558f5cd08f
Access comprehensive regulatory information for "Intermedi" Andu laser diode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f2a6e429bf99aa4ff96f3558f5cd08f and manufactured by INTERMEDIC ARFRAN, S.A.. The authorized representative in Taiwan is Yifeng International Enterprises Limited.
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
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
Nov 09, 2011
Nov 09, 2016
Mar 14, 2016
Cancellation Information
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