Taiwan FDA registration c96c6af50e099be6e9b14315a3aac0c0
Vesselcare Diagnostic Ultrasonic System
TW: 維斯科超音波診斷系統
Taiwan·Risk Class 2·MD·Qiaolian Technology Co., Ltd. Nankan Factory·Registered Feb 15, 2016 – Feb 15, 2026CancelledRegistration details
- Analysis ID
- c96c6af50e099be6e9b14315a3aac0c0
- License Form
- Ministry of Health Medical Device Manufacturing No. 005311
Company information
- Manufacturer
- Qiaolian Technology Co., Ltd. Nankan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOCARE CORPORATION
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 15, 2016
- Expiry Date
- Feb 15, 2026
- Cancellation Date
- Oct 25, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Vesselcare Diagnostic Ultrasonic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c96c6af50e099be6e9b14315a3aac0c0 and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOCARE CORPORATION.
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