Leonardo Dual Laser System - Taiwan Registration fc0db080ed505bf4c9f04ddf98229b75
Access comprehensive regulatory information for Leonardo Dual Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc0db080ed505bf4c9f04ddf98229b75 and manufactured by CeramOptec GmbH. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY 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
fc0db080ed505bf4c9f04ddf98229b75
Ministry of Health Medical Device Import No. 031921
DHA05603192107
Product Details
For details, it is Chinese approved copy of the imitation order
I General and plastic surgical devices
I4810 Lasers for general surgery, plastic surgery and dermatology
Imported from abroad
Dates and Status
Dec 10, 2018
Dec 10, 2023

