Taiwan FDA registration 9ba6debac2d27d9108d51881ffba103f
“FUJIFILM Sonosite” iViz Ultrasound System
TW: “富士索諾聲”超音波系統
Taiwan·Risk Class 2·MD·FUJIFILM SONOSITE, INC.·Registered Apr 25, 2016 – Apr 25, 2026ExpiredRegistration details
- Analysis ID
- 9ba6debac2d27d9108d51881ffba103f
- License Form
- Ministry of Health Medical Device Import No. 028518
- Customs Code
- DHA05602851805
Company information
- Manufacturer
- FUJIFILM SONOSITE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 25, 2016
- Expiry Date
- Apr 25, 2026
About this record
Access comprehensive regulatory information for “FUJIFILM Sonosite” iViz Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ba6debac2d27d9108d51881ffba103f and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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