Taiwan FDA registration a9443fd9eb2bd7202a067dbba03add27

"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 16, 2017 – Nov 16, 2027Active
Registration details
Analysis ID
a9443fd9eb2bd7202a067dbba03add27
Customs Code
DHA05603042605
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 16, 2017
Expiry Date
Nov 16, 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 a9443fd9eb2bd7202a067dbba03add27 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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