Taiwan FDA registration 617852d320eecf3d2fc7f8b5745514fc

"Fujifilm" electronic duodenoscopy and accessories

TW: “富士”電子式十二指腸鏡及附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Jun 28, 2019 – Jun 28, 2029Active
Registration details
Analysis ID
617852d320eecf3d2fc7f8b5745514fc
Customs Code
DHA05603271002
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
Jun 28, 2019
Expiry Date
Jun 28, 2029
About this record

Access comprehensive regulatory information for "Fujifilm" electronic duodenoscopy 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 617852d320eecf3d2fc7f8b5745514fc 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