"Fujifilm" endoscope accessory (unsterilized)
Taiwan·Risk Class 1·FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION·Registered Nov 10, 2020 – Nov 10, 2025Expired- Analysis ID
- 833f108489b7289f47bd7661cf137d8f
- Customs Code
- DHA09402209802
- Manufacturer
- FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- 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.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Input;; QMS/QSD
- Registration Date
- Nov 10, 2020
- Expiry Date
- Nov 10, 2025
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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.