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"Fujifilm Film" digital fluoroscopic photography imaging device - Taiwan Registration 5084a82499e647ee916c961b8ddcca67

Access comprehensive regulatory information for "Fujifilm Film" digital fluoroscopic photography imaging device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5084a82499e647ee916c961b8ddcca67 and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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5084a82499e647ee916c961b8ddcca67
Registration Details
Taiwan FDA Registration: 5084a82499e647ee916c961b8ddcca67
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Device Details

"Fujifilm Film" digital fluoroscopic photography imaging device
TW: โ€œๅฏŒๅฃซ่ปŸ็‰‡โ€ๆ•ธไฝ้€่ฆ–ๆ”ๅฝฑๆˆๅƒ่ฃ็ฝฎ
Risk Class 2

Registration Details

5084a82499e647ee916c961b8ddcca67

DHAS5603553800

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1730 ็…ง็›ธ้€่ฆ–Xๅ…‰็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jul 20, 2022

Jul 20, 2027