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"Fujifilm" console software - Taiwan Registration 9232c869dd948772ae012b0d332ae93b

Access comprehensive regulatory information for "Fujifilm" console software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9232c869dd948772ae012b0d332ae93b and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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9232c869dd948772ae012b0d332ae93b
Registration Details
Taiwan FDA Registration: 9232c869dd948772ae012b0d332ae93b
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Device Details

"Fujifilm" console software
TW: โ€œๅฏŒๅฃซโ€ ๆŽงๅˆถๅฐ่ปŸ้ซ”
Risk Class 2

Registration Details

9232c869dd948772ae012b0d332ae93b

DHA05603451906

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.2050 Medical image management and processing systems

import

Dates and Status

May 10, 2021

May 10, 2026