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"Fujifilm" electronic lower gastrointestinal endoscope and accessories - Taiwan Registration 4ba3781e08ca8dd2c1f75982b3dae3a1

Access comprehensive regulatory information for "Fujifilm" electronic lower gastrointestinal 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 4ba3781e08ca8dd2c1f75982b3dae3a1 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, 2 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION, and 5 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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4ba3781e08ca8dd2c1f75982b3dae3a1
Registration Details
Taiwan FDA Registration: 4ba3781e08ca8dd2c1f75982b3dae3a1
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Device Details

"Fujifilm" electronic lower gastrointestinal endoscope and accessories
TW: โ€œๅฏŒๅฃซโ€้›ปๅญๅผไธ‹ๆถˆๅŒ–้“ๅ…ง่ฆ–้กๅŠ้™„ไปถ
Risk Class 2

Registration Details

4ba3781e08ca8dd2c1f75982b3dae3a1

DHA05603482309

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

Aug 19, 2021

Aug 19, 2026