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"Fujifilm" digital X-ray photography system - Taiwan Registration 2ab22a0353362fb9882cb5673f78ddb4

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 2ab22a0353362fb9882cb5673f78ddb4 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 3 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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2ab22a0353362fb9882cb5673f78ddb4
Registration Details
Taiwan FDA Registration: 2ab22a0353362fb9882cb5673f78ddb4
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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

2ab22a0353362fb9882cb5673f78ddb4

DHAS0602447001

Company Information

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

import

Dates and Status

Feb 07, 2013

Feb 07, 2018

Dec 13, 2019

Cancellation Information

Logged out

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