Taiwan FDA registration 8c5c403db84c8be801a0e2c8c9ebb17c
“Misonix” SonaStar FS-1000 RF Ultrasonic Aspiration System
TW: “秘杉思”超音波手術裝置
Taiwan·Risk Class 2·MD·MISONIX, INC·Registered Oct 19, 2016 – Oct 19, 2026ActiveRegistration details
- Analysis ID
- 8c5c403db84c8be801a0e2c8c9ebb17c
- License Form
- Ministry of Health Medical Device Import No. 028994
- Customs Code
- DHA05602899401
Company information
- Manufacturer
- MISONIX, INC
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MEDICAL INSTRUMENT 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)
- I0003 Ultrasound surgical device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 19, 2016
- Expiry Date
- Oct 19, 2026
About this record
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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