Taiwan FDA registration 9232c869dd948772ae012b0d332ae93b

"Fujifilm" console software

TW: “富士” 控制台軟體

Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered May 10, 2021 – May 10, 2026Expired

Registration details

Analysis ID: 9232c869dd948772ae012b0d332ae93b
Customs Code: DHA05603451906

Company information

Manufacturer: FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION
Manufacturer Country: Japan
Authorized Representative: FUJIFILM HEALTHCARE TAIWAN CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
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: May 10, 2021
Expiry Date: May 10, 2026

About this record

Access comprehensive regulatory information for "Fujifilm" console software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9232c869dd948772ae012b0d332ae93b 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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