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"Fujifilm" ultrasound endoscope and accessories - Taiwan Registration 6a446516f34cd4d6aa96810906ba9f74

Access comprehensive regulatory information for "Fujifilm" ultrasound endoscope and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6a446516f34cd4d6aa96810906ba9f74 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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6a446516f34cd4d6aa96810906ba9f74
Registration Details
Taiwan FDA Registration: 6a446516f34cd4d6aa96810906ba9f74
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Device Details

"Fujifilm" ultrasound endoscope and accessories
TW: โ€œๅฏŒๅฃซโ€่ถ…้Ÿณๆณขๅ…ง่ฆ–้กๅŠ้™„ไปถ
Risk Class 2

Registration Details

6a446516f34cd4d6aa96810906ba9f74

DHA05603592509

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Oct 07, 2022

Oct 07, 2027