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"Fujifilm" electronic lower gastrointestinal endoscope - Taiwan Registration 0e5dde714bc14eaf6799df8330420cac

Access comprehensive regulatory information for "Fujifilm" electronic lower gastrointestinal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e5dde714bc14eaf6799df8330420cac and manufactured by FUJIFILM Techno Products Co., Ltd. Mito Site;; 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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0e5dde714bc14eaf6799df8330420cac
Registration Details
Taiwan FDA Registration: 0e5dde714bc14eaf6799df8330420cac
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Device Details

"Fujifilm" electronic lower gastrointestinal endoscope
TW: โ€œๅฏŒๅฃซโ€้›ปๅญไธ‹ๆถˆๅŒ–้“ๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

0e5dde714bc14eaf6799df8330420cac

DHA05602822503

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Mar 14, 2016

Mar 14, 2026