Taiwan FDA registration 1012b24571478b82914e60d822017bbd

Fujifilm Medical X-ray Film (Unsterilized)

TW: “富士”醫療用X光軟片 (未滅菌)

Taiwan·Risk Class 1·FUJIFILM Material Manufacturing Co.,Ltd. Shizuoka Area.;; FUJIFILM CORPORATION·Registered Jun 19, 2013 – Jun 19, 2028Active

Registration details

Analysis ID: 1012b24571478b82914e60d822017bbd
Customs Code: DHA04401312001

Company information

Manufacturer: FUJIFILM Material Manufacturing Co.,Ltd. Shizuoka Area.;; FUJIFILM CORPORATION
Manufacturer Country: Japan
Authorized Representative: FUJIFILM HEALTHCARE TAIWAN CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Radiation Film (P.1840)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1840 Radiographic film
Import Information: import

Dates and status

Registration Date: Jun 19, 2013
Expiry Date: Jun 19, 2028

About this record

Access comprehensive regulatory information for Fujifilm Medical X-ray Film (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1012b24571478b82914e60d822017bbd and manufactured by FUJIFILM Material Manufacturing Co.,Ltd. Shizuoka Area.;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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