Taiwan FDA registration d4f9557e35882c5562641e137718b735
“NEWPONG” sonoQueen Focused Ultrasound Stimulator use System
TW: “紐朋”聚焦超音波治療系統
Taiwan·Risk Class 2·MD·NEWPONG Co., Ltd·Registered Feb 18, 2022 – Feb 18, 2027ActiveRegistration details
- Analysis ID
- d4f9557e35882c5562641e137718b735
- License Form
- Ministry of Health Medical Device Import No. 035273
- Customs Code
- DHA05603527305
Company information
- Manufacturer
- NEWPONG Co., Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- WOH MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4590 Focused Ultrasound Stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 18, 2022
- Expiry Date
- Feb 18, 2027
About this record
Access comprehensive regulatory information for “NEWPONG” sonoQueen Focused Ultrasound Stimulator use System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4f9557e35882c5562641e137718b735 and manufactured by NEWPONG Co., Ltd. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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