Taiwan FDA registration 090c30d355746ce26daffff7d8521719

Fujifilm computer X-ray imaging system

TW: “富士” 電腦X光影像系統
Taiwan flagTaiwan·Risk Class 2·FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.·Registered Dec 18, 2012 – Dec 18, 2017Cancelled
Registration details
Analysis ID
090c30d355746ce26daffff7d8521719
Customs Code
DHA04200046508
Company information
Manufacturer Country
China
Authorized Representative
NAN KAI CORPORATION
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.1650 透視X光影像增感管
Import Information
Chinese goods;; input
Dates and status
Registration Date
Dec 18, 2012
Expiry Date
Dec 18, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
Companies making similar products

Top companies providing products similar to "Fujifilm computer X-ray imaging system"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for Fujifilm computer X-ray imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 090c30d355746ce26daffff7d8521719 and manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.. The authorized representative in Taiwan is NAN KAI CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.;; FUJIFILM CORPORATION, and 1 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations