Taiwan FDA registration 582e2a1e3ead4666711565d588894c96
“FUJIFILM SonoSite” Edge Diagnostic Doppler Ultrasound System
TW: “富士索諾聲”數位彩色超音波掃描器
Taiwan·Risk Class 2·MD·FUJIFILM SONOSITE, INC.·Registered Mar 25, 2014 – Mar 25, 2024ExpiredRegistration details
- Analysis ID
- 582e2a1e3ead4666711565d588894c96
- License Form
- Ministry of Health Medical Device Import No. 026025
- Customs Code
- DHA05602602501
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 25, 2014
- Expiry Date
- Mar 25, 2024
About this record
Access comprehensive regulatory information for “FUJIFILM SonoSite” Edge Diagnostic Doppler 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 582e2a1e3ead4666711565d588894c96 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