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"Fujifilm" electronic bronchoscope and accessories - Taiwan Registration 0afcfdf802ccc73b512a60a7ac88747f

Access comprehensive regulatory information for "Fujifilm" electronic bronchoscope and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0afcfdf802ccc73b512a60a7ac88747f 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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0afcfdf802ccc73b512a60a7ac88747f
Registration Details
Taiwan FDA Registration: 0afcfdf802ccc73b512a60a7ac88747f
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Device Details

"Fujifilm" electronic bronchoscope and accessories
TW: โ€œๅฏŒๅฃซโ€้›ปๅญๅผๆ”ฏๆฐฃ็ฎก้กๅŠ้™„ไปถ
Risk Class 2

Registration Details

0afcfdf802ccc73b512a60a7ac88747f

DHA05603497302

Product Details

Details are as detailed as approved Chinese instructions

G ENT Science

G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof

import

Dates and Status

Oct 13, 2021

Oct 13, 2026