Taiwan FDA registration dcc38b24c5324d4b7efe14ed7df84b07

"Fujifilm" airbag controller

TW: “富士”氣囊控制器

Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Apr 22, 2019 – Apr 22, 2029Active

Registration details

Analysis ID: dcc38b24c5324d4b7efe14ed7df84b07
Customs Code: DHA05603252109

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: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: import

Dates and status

Registration Date: Apr 22, 2019
Expiry Date: Apr 22, 2029

About this record

Access comprehensive regulatory information for "Fujifilm" airbag controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcc38b24c5324d4b7efe14ed7df84b07 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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