Taiwan FDA registration 8b0e12015889ea266ebbb267061ae373

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.;; FUJIFILM CORPORATION·Registered Mar 04, 2013 – Mar 04, 2028Active
Registration details
Analysis ID
8b0e12015889ea266ebbb267061ae373
Customs Code
DHA04200050000
Company information
Manufacturer Country
Japan;;China
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.1650 透視X光影像增感管
Import Information
Chinese goods;; input
Dates and status
Registration Date
Mar 04, 2013
Expiry Date
Mar 04, 2028
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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 8b0e12015889ea266ebbb267061ae373 and manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.;; 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 IMAGING SYSTEMS (SUZHOU) CO., LTD., 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.

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