Taiwan FDA registration 6fcf2bd05bbcbad33c091aead5471af4
“FUJIFILM Sonosite” SII Ultrasound System
TW: “富士索諾聲”超音波系統
Taiwan·Risk Class 2·MD·FUJIFILM SONOSITE, INC.·Registered Mar 30, 2017 – Mar 30, 2027ActiveRegistration details
- Analysis ID
- 6fcf2bd05bbcbad33c091aead5471af4
- License Form
- Ministry of Health Medical Device Import No. 029429
- Customs Code
- DHA05602942901
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
- Mar 30, 2017
- Expiry Date
- Mar 30, 2027
About this record
Access comprehensive regulatory information for “FUJIFILM Sonosite” SII 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 6fcf2bd05bbcbad33c091aead5471af4 and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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