Taiwan FDA registration 739713388f8743fce42fd8639777a041

Fujifilm digital mammography computer-aided detection application

TW: “富士”數位乳房攝影電腦輔助偵測應用軟體
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered Oct 17, 2017 – Oct 17, 2027Active
Registration details
Analysis ID
739713388f8743fce42fd8639777a041
Customs Code
DHA05603028806
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
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.2050 Medical image management and processing systems
Import Information
import
Dates and status
Registration Date
Oct 17, 2017
Expiry Date
Oct 17, 2027
About this record

Access comprehensive regulatory information for Fujifilm digital mammography computer-aided detection application in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 739713388f8743fce42fd8639777a041 and manufactured by FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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