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“NEWPONG” sonoQueen Focused Ultrasound Stimulator use System - Taiwan Registration d4f9557e35882c5562641e137718b735

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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d4f9557e35882c5562641e137718b735
Registration Details
Taiwan FDA Registration: d4f9557e35882c5562641e137718b735
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Device Details

“NEWPONG” sonoQueen Focused Ultrasound Stimulator use System
TW: “紐朋”聚焦超音波治療系統
Risk Class 2
MD

Registration Details

d4f9557e35882c5562641e137718b735

Ministry of Health Medical Device Import No. 035273

DHA05603527305

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4590 Focused Ultrasound Stimulator

Imported from abroad

Dates and Status

Feb 18, 2022

Feb 18, 2027