"K.F." CURING SHEET - Taiwan Registration 68687ead60f4dda28981be690fceb6a2
Access comprehensive regulatory information for "K.F." CURING SHEET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68687ead60f4dda28981be690fceb6a2 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Guofa Medical Equipment 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
68687ead60f4dda28981be690fceb6a2
Department of Health Medical Device Manufacturing No. 001737
DHY00500173702
Product Details
For details, it is Chinese approved copy of the imitation order
I General and plastic surgical devices
Produced in Taiwan, China
Dates and Status
Apr 03, 2006
Apr 03, 2026

