Taiwan FDA registration 23a8bf8d4a579fc8e9f52d3347279a28

"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 Nov 09, 2007 – Nov 09, 2022Cancelled
Registration details
Analysis ID
23a8bf8d4a579fc8e9f52d3347279a28
Customs Code
DHA00601844008
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.1630 靜電式X光影像系統
Import Information
import
Dates and status
Registration Date
Nov 09, 2007
Expiry Date
Nov 09, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 23a8bf8d4a579fc8e9f52d3347279a28 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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