Taiwan FDA registration 3fe643601b23d946874e486d83dae3c9
“KONICA MINOLTA”Direct Digitizer SKR 3000
TW: “柯尼卡美能達”數位X光成像系統
Taiwan·Risk Class 2·MD·Konica Minolta Technoproducts Co., Ltd.·Registered Jun 28, 2022 – Jun 28, 2027ActiveRegistration details
- Analysis ID
- 3fe643601b23d946874e486d83dae3c9
- License Form
- Ministry of Health Medical Device Import No. 035514
- Customs Code
- DHA05603551401
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)
- P1650 fluoroscopic X-ray image intensifier
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 28, 2022
- Expiry Date
- Jun 28, 2027
About this record
Access comprehensive regulatory information for “KONICA MINOLTA”Direct Digitizer SKR 3000 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fe643601b23d946874e486d83dae3c9 and manufactured by Konica Minolta Technoproducts Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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