“Jeisys” Focused Ultrasound Stimulator Use System and Electrosurgical Unit - Taiwan Registration 10f421dbe304822a30e00b7cc10740cd
Access comprehensive regulatory information for “Jeisys” Focused Ultrasound Stimulator Use System and Electrosurgical Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 10f421dbe304822a30e00b7cc10740cd and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY 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
10f421dbe304822a30e00b7cc10740cd
Ministry of Health Medical Device Import No. 028590
DHA05602859000
Product Details
For details, it is Chinese approved copy of the imitation order
I General and plastic surgical devices
I4400 Electric knife for cutting and hemostasis and its accessories;;I0003 Ultrasound surgical device
Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
Dates and Status
May 23, 2016
May 23, 2026

