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"Fujifilm" endoscope accessory (unsterilized) - Taiwan Registration 833f108489b7289f47bd7661cf137d8f

Access comprehensive regulatory information for "Fujifilm" endoscope accessory (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 833f108489b7289f47bd7661cf137d8f and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION, and 1 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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833f108489b7289f47bd7661cf137d8f
Registration Details
Taiwan FDA Registration: 833f108489b7289f47bd7661cf137d8f
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Device Details

"Fujifilm" endoscope accessory (unsterilized)
TW: โ€œๅฏŒๅฃซโ€ ๅ…ง่ฆ–้ก้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

833f108489b7289f47bd7661cf137d8f

DHA09402209802

Product Details

Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Input;; QMS/QSD

Dates and Status

Nov 10, 2020

Nov 10, 2025

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