Taiwan FDA registration 07c206ba301985e97d6ecd4f25abb1b6

"Fujifilm Film" digital fluoroscopic photography X-ray installation

TW: “富士軟片”數位透視攝影X光裝置
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa·Registered Oct 01, 2009 – Oct 01, 2029Active
Registration details
Analysis ID
07c206ba301985e97d6ecd4f25abb1b6
Customs Code
DHAS0602021909
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.1730 照相透視X光系統
Import Information
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Oct 01, 2009
Expiry Date
Oct 01, 2029
About this record

Access comprehensive regulatory information for "Fujifilm Film" digital fluoroscopic photography X-ray installation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07c206ba301985e97d6ecd4f25abb1b6 and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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