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"Fujifilm" digital X-ray photography system - Taiwan Registration d892b9eeca45f4b958f24a2f63b76cdf

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 d892b9eeca45f4b958f24a2f63b76cdf and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION, 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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d892b9eeca45f4b958f24a2f63b76cdf
Registration Details
Taiwan FDA Registration: d892b9eeca45f4b958f24a2f63b76cdf
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Device Details

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

Registration Details

d892b9eeca45f4b958f24a2f63b76cdf

DHA00602205303

Product Details

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

P Radiology Science

P.1630 ้œ้›ปๅผXๅ…‰ๅฝฑๅƒ็ณป็ตฑ

import

Dates and Status

Feb 09, 2011

Feb 09, 2021

Sep 19, 2023

Cancellation Information

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