Taiwan FDA registration 869821382f1ec119c5b2644d3ad9e8fc

"Konica Minolta" medical imaging digitizer

TW: “柯尼卡美能達” 醫學影像數位器
Taiwan flagTaiwan·Risk Class 2·KONICA MINOLTA TECHNOPRODUCTS CO., LTD.·Registered Oct 03, 2011 – Oct 03, 2016Cancelled
Registration details
Analysis ID
869821382f1ec119c5b2644d3ad9e8fc
Customs Code
DHA00602283000
Company information
Manufacturer Country
Japan
Authorized Representative
MEDEPOCH TRADING 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
import
Dates and status
Registration Date
Oct 03, 2011
Expiry Date
Oct 03, 2016
Cancellation Date
Aug 21, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Konica Minolta" medical imaging digitizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 869821382f1ec119c5b2644d3ad9e8fc and manufactured by KONICA MINOLTA TECHNOPRODUCTS CO., LTD.. The authorized representative in Taiwan is MEDEPOCH TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KONICA MINOLTA TECHNOPRODUCTS CO., LTD., 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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