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"Fujifilm" endoscopic ultrasound host - Taiwan Registration 50e039a69809e3363a9e87bbf424605d

Access comprehensive regulatory information for "Fujifilm" endoscopic ultrasound host in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50e039a69809e3363a9e87bbf424605d and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE, and 1 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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50e039a69809e3363a9e87bbf424605d
Registration Details
Taiwan FDA Registration: 50e039a69809e3363a9e87bbf424605d
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Device Details

"Fujifilm" endoscopic ultrasound host
TW: โ€œๅฏŒๅฃซโ€ๅ…ง่ฆ–้ก่ถ…้ŸณๆณขไธปๆฉŸ
Risk Class 2

Registration Details

50e039a69809e3363a9e87bbf424605d

DHA05602914701

Product Details

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

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Dec 20, 2016

Dec 20, 2026

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