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"Fujifilm" electronic lower gastrointestinal endoscope and accessories - Taiwan Registration d70b0a927a1a310aaa4b2f5806d03aac

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 d70b0a927a1a310aaa4b2f5806d03aac 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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d70b0a927a1a310aaa4b2f5806d03aac
Registration Details
Taiwan FDA Registration: d70b0a927a1a310aaa4b2f5806d03aac
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Device Details

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

Registration Details

d70b0a927a1a310aaa4b2f5806d03aac

DHA05603270009

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

Jun 22, 2019

Jun 22, 2029