Taiwan FDA registration 15aec7e6c091ff485f7eb40f661e3ecc

"Fujifilm" endoscope accessory (unsterilized)

TW: “富士” 內視鏡附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Sep 25, 2020 – Sep 25, 2025Expired
Registration details
Analysis ID
15aec7e6c091ff485f7eb40f661e3ecc
Customs Code
DHA09402198508
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
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
import
Dates and status
Registration Date
Sep 25, 2020
Expiry Date
Sep 25, 2025
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About this record

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 15aec7e6c091ff485f7eb40f661e3ecc and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki 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 Hitachiomiya 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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