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Fujifilm endoscopic ultrasound probe - Taiwan Registration b2e008bb79b5f5a715a6b07de3ca230e

Access comprehensive regulatory information for Fujifilm endoscopic ultrasound probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b2e008bb79b5f5a715a6b07de3ca230e 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. 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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b2e008bb79b5f5a715a6b07de3ca230e
Registration Details
Taiwan FDA Registration: b2e008bb79b5f5a715a6b07de3ca230e
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Device Details

Fujifilm endoscopic ultrasound probe
TW: โ€œๅฏŒๅฃซโ€ๅ…ง่ฆ–้ก่ถ…้ŸณๆณขๆŽข้ ญ
Risk Class 2

Registration Details

b2e008bb79b5f5a715a6b07de3ca230e

DHA05603608700

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1570 ่จบๆ–ท็”จ่ถ…้Ÿณๆณข่ฝ‰ๆ›ๅ™จ

import

Dates and Status

Jan 17, 2023

Jan 17, 2028