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"Fujifilm" endoscopic ultrasound host - Taiwan Registration cae5a442c830b43c8ff89c77f9ca7911

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 cae5a442c830b43c8ff89c77f9ca7911 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. 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 Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, 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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cae5a442c830b43c8ff89c77f9ca7911
Registration Details
Taiwan FDA Registration: cae5a442c830b43c8ff89c77f9ca7911
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Device Details

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

Registration Details

cae5a442c830b43c8ff89c77f9ca7911

DHA00602352602

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

Jun 05, 2012

Jun 05, 2022

Apr 12, 2024

Cancellation Information

Logged out

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