Taiwan FDA registration 14254bf5fc44caa16d90568ae6d8431e

"Fujifilm" electronic digestive endoscope and its accessories

TW: “富士”電子消化道內視鏡及其附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Oct 29, 2020 – Oct 29, 2025Expired
Registration details
Analysis ID
14254bf5fc44caa16d90568ae6d8431e
Customs Code
DHA05603400807
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
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
Oct 29, 2020
Expiry Date
Oct 29, 2025
About this record

Access comprehensive regulatory information for "Fujifilm" electronic digestive endoscope and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14254bf5fc44caa16d90568ae6d8431e 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. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices