Taiwan FDA registration 4b861bbbef41a9aac7a9c0e6d00e6066
“KONICA MINOLTA” ULTRASOUND SYSTYEM
TW: “柯尼卡美能達”超音波系統
Taiwan·Risk Class 2·MD·Konica Minolta Technoproducts Co., Ltd.·Registered Sep 21, 2017 – Sep 21, 2027ActiveRegistration details
- Analysis ID
- 4b861bbbef41a9aac7a9c0e6d00e6066
- License Form
- Ministry of Health Medical Device Import No. 030256
- Customs Code
- DHA05603025606
Company information
- Manufacturer
- Konica Minolta Technoproducts Co., Ltd.
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 21, 2017
- Expiry Date
- Sep 21, 2027
About this record
Access comprehensive regulatory information for “KONICA MINOLTA” ULTRASOUND SYSTYEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b861bbbef41a9aac7a9c0e6d00e6066 and manufactured by Konica Minolta Technoproducts Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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