Taiwan FDA registration 10f421dbe304822a30e00b7cc10740cd
“Jeisys” Focused Ultrasound Stimulator Use System and Electrosurgical Unit
TW: “婕曦”超音波及電刀系統
Taiwan·Risk Class 2·MD·Jeisys Medical Inc.·Registered May 23, 2016 – May 23, 2026ExpiredRegistration details
- Analysis ID
- 10f421dbe304822a30e00b7cc10740cd
- License Form
- Ministry of Health Medical Device Import No. 028590
- Customs Code
- DHA05602859000
Company information
- Manufacturer
- Jeisys Medical Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YUNGLIN BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories;;I0003 Ultrasound surgical device
- Import Information
- 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
- Registration Date
- May 23, 2016
- Expiry Date
- May 23, 2026
About this record
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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