Taiwan FDA registration 53f2ead7552b37d29d9a90fd1d8fcc7b
“FUJIFILM” Workstation AMULET Bellus Software
TW: “富士”乳房影像工作站軟體
Taiwan·Risk Class 2·MD·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Sep 10, 2015 – Sep 10, 2020CancelledRegistration details
- Analysis ID
- 53f2ead7552b37d29d9a90fd1d8fcc7b
- License Form
- Ministry of Health Medical Device Import No. 027728
- Customs Code
- DHA05602772801
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 2015
- Expiry Date
- Sep 10, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “FUJIFILM” Workstation AMULET Bellus Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53f2ead7552b37d29d9a90fd1d8fcc7b and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
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