Taiwan FDA registration aeca4ec33dae512904be5c1d02fba1cf

"Fujifilm" mobile digital X-ray photography system and accessories

TW: “富士”移動式數位X光攝影系統及配件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Jul 16, 2019 – Jul 16, 2029Active
Registration details
Analysis ID
aeca4ec33dae512904be5c1d02fba1cf
Customs Code
DHAS5603266502
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.1720 移動式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
Jul 16, 2019
Expiry Date
Jul 16, 2029
About this record

Access comprehensive regulatory information for "Fujifilm" mobile digital X-ray photography system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aeca4ec33dae512904be5c1d02fba1cf and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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