Taiwan FDA registration 4fe90ede6b495e09272c136321efcb08

"Fujifilm" digital X-ray photography system

TW: “富士”數位X光攝影系統
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Jul 07, 2022 – Jul 07, 2027Active
Registration details
Analysis ID
4fe90ede6b495e09272c136321efcb08
Customs Code
DHA05603552200
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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
Jul 07, 2022
Expiry Date
Jul 07, 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 4fe90ede6b495e09272c136321efcb08 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki 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 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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