Taiwan FDA registration e3dee9bf191ee29ec4a9fc8f0fb8a744
“KONICA MINOLTA” Imaging Diagnostic Workstation DI-X1
TW: “柯尼卡美能達” 影像診斷工作站
Taiwan·Risk Class 2·MD·Konica Minolta Technoproducts Co., Ltd.·Registered Apr 04, 2023 – Apr 04, 2028ActiveRegistration details
- Analysis ID
- e3dee9bf191ee29ec4a9fc8f0fb8a744
- License Form
- Ministry of Health Medical Device Import No. 036342
- Customs Code
- DHA05603634203
Company information
- Manufacturer
- Konica Minolta Technoproducts Co., Ltd.
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 04, 2023
- Expiry Date
- Apr 04, 2028
About this record
Access comprehensive regulatory information for “KONICA MINOLTA” Imaging Diagnostic Workstation DI-X1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3dee9bf191ee29ec4a9fc8f0fb8a744 and manufactured by Konica Minolta Technoproducts Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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