Taiwan FDA registration 0f050fd16099b66b8b6312cc183516a8

"Fujifilm" endoscope accessories (sterilized/unsterilized)

TW: “富士” 內視鏡附件 (滅菌/未滅菌)

Taiwan·Risk Class 1·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Aug 24, 2020 – Aug 24, 2025Expired

Registration details

Analysis ID: 0f050fd16099b66b8b6312cc183516a8
Customs Code: DHA09402189102

Company information

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

Product details

Intended Use: Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Aug 24, 2020
Expiry Date: Aug 24, 2025

About this record

Access comprehensive regulatory information for "Fujifilm" endoscope accessories (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0f050fd16099b66b8b6312cc183516a8 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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