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"Fujifilm" digital X-ray photography system - Taiwan Registration fe40d786cbe5b710aa549cf3397134c0

Access comprehensive regulatory information for "Fujifilm" digital X-ray photography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe40d786cbe5b710aa549cf3397134c0 and manufactured by FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE, and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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fe40d786cbe5b710aa549cf3397134c0
Registration Details
Taiwan FDA Registration: fe40d786cbe5b710aa549cf3397134c0
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Device Details

"Fujifilm" digital X-ray photography system
TW: โ€œๅฏŒๅฃซโ€ๆ•ธไฝXๅ…‰ๆ”ๅฝฑ็ณป็ตฑ
Risk Class 2

Registration Details

fe40d786cbe5b710aa549cf3397134c0

DHA05602760202

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

import

Dates and Status

Aug 19, 2015

Aug 19, 2025