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"Fujifilm" electronic digestive endoscope and its accessories - Taiwan Registration 14254bf5fc44caa16d90568ae6d8431e

Access comprehensive regulatory information for "Fujifilm" electronic digestive endoscope and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14254bf5fc44caa16d90568ae6d8431e 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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14254bf5fc44caa16d90568ae6d8431e
Registration Details
Taiwan FDA Registration: 14254bf5fc44caa16d90568ae6d8431e
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Device Details

"Fujifilm" electronic digestive endoscope and its accessories
TW: โ€œๅฏŒๅฃซโ€้›ปๅญๆถˆๅŒ–้“ๅ…ง่ฆ–้กๅŠๅ…ถ้™„ไปถ
Risk Class 2

Registration Details

14254bf5fc44caa16d90568ae6d8431e

DHA05603400807

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Oct 29, 2020

Oct 29, 2025