Taiwan FDA registration 4dec3935d8844ec27f45f68f6a3e1abc
"Ultraimage" ultrasonic imaging system
TW: “超象” 超音波影像系統
Taiwan·Risk Class 2·Chaoxiang Technology Co., Ltd.; Qingwang Technology Co., Ltd·Registered Dec 26, 2019 – Dec 26, 2029ActiveRegistration details
- Analysis ID
- 4dec3935d8844ec27f45f68f6a3e1abc
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LELTEK INC.
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.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Dec 26, 2019
- Expiry Date
- Dec 26, 2029
About this record
Access comprehensive regulatory information for "Ultraimage" ultrasonic imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dec3935d8844ec27f45f68f6a3e1abc and manufactured by Chaoxiang Technology Co., Ltd.; Qingwang Technology Co., Ltd. The authorized representative in Taiwan is LELTEK INC..
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