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“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..

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10f421dbe304822a30e00b7cc10740cd
Registration Details
Taiwan FDA Registration: 10f421dbe304822a30e00b7cc10740cd
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Device Details

“Jeisys” Focused Ultrasound Stimulator Use System and Electrosurgical Unit
TW: “婕曦”超音波及電刀系統
Risk Class 2
MD

Registration Details

10f421dbe304822a30e00b7cc10740cd

Ministry of Health Medical Device Import No. 028590

DHA05602859000

Company Information

Korea, Republic of

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