Taiwan FDA registration 33dbec6bca03adf27b7d4e951f698fee
“Misonix” neXus Ultrasonic Surgical Aspirator System
TW: “秘杉思”紐克斯超音波手術抽吸裝置
Taiwan·Risk Class 2·MD·MISONIX, INC·Registered Jun 13, 2021 – Jun 13, 2026ExpiredRegistration details
- Analysis ID
- 33dbec6bca03adf27b7d4e951f698fee
- License Form
- Ministry of Health Medical Device Import No. 034597
- Customs Code
- DHA05603459700
Company information
- Manufacturer
- MISONIX, INC
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jun 13, 2021
- Expiry Date
- Jun 13, 2026
About this record
Access comprehensive regulatory information for “Misonix” neXus Ultrasonic Surgical Aspirator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 33dbec6bca03adf27b7d4e951f698fee and manufactured by MISONIX, INC. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices