Taiwan FDA registration 7f10ec6884d0555d28d2b59497d9e68f

"Fujifilm" digital X-ray photography system

TW: “富士”數位X光攝影系統
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered Nov 27, 2017 – Nov 27, 2027Active
Registration details
Analysis ID
7f10ec6884d0555d28d2b59497d9e68f
Customs Code
DHA05603044509
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)
P Radiology Science
Product Type (Level 2)
P.1680 固定式X光系統
Import Information
import
Dates and status
Registration Date
Nov 27, 2017
Expiry Date
Nov 27, 2027
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About this record

Access comprehensive regulatory information for "Fujifilm" digital X-ray photography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f10ec6884d0555d28d2b59497d9e68f and manufactured by FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including FUJIFILM Corporation;; FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, FUJIFILM TECHNO PRODUCTS CO., LTD. TOUHOKU FACTORY HANAMAKI SITE, 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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