Taiwan FDA registration 89d2105f8096fbc07b72de7a0388babe
“FUJIFILM Sonosite” Edge II Ultrasound System
TW: “富士索諾聲”超音波系統
Taiwan·Risk Class 2·MD·FUJIFILM SONOSITE, INC.·Registered Mar 22, 2017 – Mar 22, 2027ActiveRegistration details
- Analysis ID
- 89d2105f8096fbc07b72de7a0388babe
- License Form
- Ministry of Health Medical Device Import No. 029419
- Customs Code
- DHA05602941908
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 22, 2017
- Expiry Date
- Mar 22, 2027
About this record
Access comprehensive regulatory information for “FUJIFILM Sonosite” Edge II 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 89d2105f8096fbc07b72de7a0388babe and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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