Taiwan FDA registration 41d6b4f3ec12fbd1a9861d6525f6909f

"Fujifilm" electronic lower gastrointestinal endoscope and accessories

TW: “富士”電子下消化道內視鏡及附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION·Registered Jun 22, 2015 – Jun 22, 2025Expired
Registration details
Analysis ID
41d6b4f3ec12fbd1a9861d6525f6909f
Customs Code
DHA05602747702
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 22, 2015
Expiry Date
Jun 22, 2025
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About this record

Access comprehensive regulatory information for "Fujifilm" electronic lower 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 41d6b4f3ec12fbd1a9861d6525f6909f 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 Sano Office;; 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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