Taiwan FDA registration 91b18d439f2d01e2635c9b0d9e6aa829

"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 Sep 15, 2011 – Sep 15, 2026Active
Registration details
Analysis ID
91b18d439f2d01e2635c9b0d9e6aa829
Customs Code
DHA00602280600
Company information
Manufacturer Country
Japan
Authorized Representative
QUALTECH CONSULTING 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
import
Dates and status
Registration Date
Sep 15, 2011
Expiry Date
Sep 15, 2026
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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 91b18d439f2d01e2635c9b0d9e6aa829 and manufactured by KONICA MINOLTA TECHNOPRODUCTS CO., LTD.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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