Taiwan FDA registration 154f85a9ba5addc42d33f2eb28b589e2
"Jiastar " ultrasonic system
TW: “佳世達”超音波系統
Taiwan·Risk Class 2·Jiastar Technology Co., Ltd. Double Star Factory 2·Registered Dec 10, 2013 – Dec 10, 2023ExpiredRegistration details
- Analysis ID
- 154f85a9ba5addc42d33f2eb28b589e2
- Customs Code
- DHA05500429803
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jiastar Technology Co., Ltd. Double Star Factory 2
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1570 Ultrasound converters for diagnostic use;; P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- Medical equipment produced in bonded factories; Domestic
Dates and status
- Registration Date
- Dec 10, 2013
- Expiry Date
- Dec 10, 2023
About this record
Access comprehensive regulatory information for "Jiastar " 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 154f85a9ba5addc42d33f2eb28b589e2 and manufactured by Jiastar Technology Co., Ltd. Double Star Factory 2. The authorized representative in Taiwan is Jiastar Technology Co., Ltd. Double Star Factory 2.
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