"Fuji Sono Sound" ultrasonic system
Taiwan·Risk Class 2·FUJIFILM Sonosite, Inc.·Registered Aug 18, 2024 – Aug 18, 2029Active- Analysis ID
- a44fd0ea5b222f44ae65f0c4fbe1dad1
- Customs Code
- DHA05603728904
- Manufacturer
- FUJIFILM Sonosite, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- EMERGO TAIWAN LIMITED
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
- Registration Date
- Aug 18, 2024
- Expiry Date
- Aug 18, 2029
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Access comprehensive regulatory information for "Fuji Sono Sound" ultrasonic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a44fd0ea5b222f44ae65f0c4fbe1dad1 and manufactured by FUJIFILM Sonosite, Inc.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM SONOSITE, INC., and 1 recent registrations in the same category. 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.