Taiwan FDA registration 345c6b8e83ed776de816a5047c0b679c

"Konica Minolta" medical imaging digital device

TW: “科尼卡美能達”醫學影像數位器
Taiwan flagTaiwan·Risk Class 2·KONICA MINOLTA TECHNOPRODUCTS CO., LTD.·Registered Jun 11, 2010 – Jun 11, 2020Cancelled
Registration details
Analysis ID
345c6b8e83ed776de816a5047c0b679c
Customs Code
DHA00602111902
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
Jun 11, 2010
Expiry Date
Jun 11, 2020
Cancellation Date
Jun 07, 2022
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 digital device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 345c6b8e83ed776de816a5047c0b679c 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 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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