Taiwan FDA registration 9d5380c74b75a370d440020388f2ebc9

"Fujifilm" electronic upper gastrointestinal endoscope and accessories

TW: “富士”電子上消化道內視鏡及附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION·Registered Jun 04, 2016 – Jun 04, 2026Expired
Registration details
Analysis ID
9d5380c74b75a370d440020388f2ebc9
Customs Code
DHA05602865808
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 04, 2016
Expiry Date
Jun 04, 2026
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About this record

Access comprehensive regulatory information for "Fujifilm" electronic upper gastrointestinal endoscope 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 9d5380c74b75a370d440020388f2ebc9 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, 3 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, FUJIFILM Techno Products Co., Ltd. Mito Site;; FUJIFILM CORPORATION, and 5 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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