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“Misonix” SonaStar FS-1000 RF Ultrasonic Aspiration System - Taiwan Registration 8c5c403db84c8be801a0e2c8c9ebb17c

Access comprehensive regulatory information for “Misonix” SonaStar FS-1000 RF Ultrasonic Aspiration System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c5c403db84c8be801a0e2c8c9ebb17c and manufactured by MISONIX, INC. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..

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8c5c403db84c8be801a0e2c8c9ebb17c
Registration Details
Taiwan FDA Registration: 8c5c403db84c8be801a0e2c8c9ebb17c
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Device Details

“Misonix” SonaStar FS-1000 RF Ultrasonic Aspiration System
TW: “秘杉思”超音波手術裝置
Risk Class 2
MD

Registration Details

8c5c403db84c8be801a0e2c8c9ebb17c

Ministry of Health Medical Device Import No. 028994

DHA05602899401

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I0003 Ultrasound surgical device

Imported from abroad

Dates and Status

Oct 19, 2016

Oct 19, 2026