Taiwan FDA registration 8c840c36c4e72562448dc7a471230fb0
"Sonosound" ultrasound imaging system and its accessories
TW: “索諾聲”超音波影像系統及其附件
Taiwan·Risk Class 2·FUJIFILM SONOSITE, INC.·Registered Jan 05, 2009 – Jan 05, 2029ActiveRegistration details
- Analysis ID
- 8c840c36c4e72562448dc7a471230fb0
- Customs Code
- DHA00601954603
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 Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
Dates and status
- Registration Date
- Jan 05, 2009
- Expiry Date
- Jan 05, 2029
About this record
Access comprehensive regulatory information for "Sonosound" ultrasound imaging system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c840c36c4e72562448dc7a471230fb0 and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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