Taiwan FDA registration e4435b495a72fd6eba33cdb5340d74ed

"Fujifilm" film box type computer X-ray image reader

TW: “富士”片匣式電腦X光影像讀取儀
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered Jul 10, 2014 – Jul 10, 2029Active
Registration details
Analysis ID
e4435b495a72fd6eba33cdb5340d74ed
Customs Code
DHA05602640001
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.1650 透視X光影像增感管
Import Information
import
Dates and status
Registration Date
Jul 10, 2014
Expiry Date
Jul 10, 2029
About this record

Access comprehensive regulatory information for "Fujifilm" film box type computer X-ray image reader in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4435b495a72fd6eba33cdb5340d74ed and manufactured by FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. 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