Taiwan FDA registration e6bc50f0c87d714f6e08f424a7f639fa

"Fujifilm" endoscope host

TW: “富士”內視鏡主機
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Nov 06, 2020 – Nov 06, 2025Expired
Registration details
Analysis ID
e6bc50f0c87d714f6e08f424a7f639fa
Customs Code
DHA05603401708
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
Nov 06, 2020
Expiry Date
Nov 06, 2025
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About this record

Access comprehensive regulatory information for "Fujifilm" endoscope host in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e6bc50f0c87d714f6e08f424a7f639fa 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, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, and 2 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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