Taiwan FDA registration 02bed52f946d532131e74e46efea3c24
“KONICA MINOLTA” DIRECT DIGITIZER
TW: “柯尼卡美能達”醫學影像數位器
Taiwan·Risk Class 2·MD·Konica Minolta Technoproducts Co., Ltd.·Registered Sep 06, 2017 – Sep 06, 2022ExpiredRegistration details
- Analysis ID
- 02bed52f946d532131e74e46efea3c24
- License Form
- Ministry of Health Medical Device Import No. 030181
- Customs Code
- DHA05603018101
Company information
- Manufacturer
- Konica Minolta Technoproducts Co., Ltd.
- 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 Devices for radiology
- Product Type (Level 2)
- P1650 fluoroscopic X-ray image intensifier
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 06, 2017
- Expiry Date
- Sep 06, 2022
About this record
Access comprehensive regulatory information for “KONICA MINOLTA” DIRECT DIGITIZER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02bed52f946d532131e74e46efea3c24 and manufactured by Konica Minolta Technoproducts Co., Ltd.. The authorized representative in Taiwan is MEDEPOCH TRADING CO., LTD..
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