Taiwan FDA registration ae5e7c82eac52c671b58538f8a1cb813
"Plusrite" flow rate development ultrasound guidance for a complete set of implantable vascular infusion
TW: “普羅斯”流速顯影超音波引導用全套式植入式血管輸注器
Taiwan·Risk Class 2·PEROUSE MEDICAL·Registered Jan 13, 2020 – Jan 13, 2030ActiveRegistration details
- Analysis ID
- ae5e7c82eac52c671b58538f8a1cb813
- Customs Code
- DHA05603320902
Company information
- Manufacturer
- PEROUSE MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- AMED CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Jan 13, 2020
- Expiry Date
- Jan 13, 2030
About this record
Access comprehensive regulatory information for "Plusrite" flow rate development ultrasound guidance for a complete set of implantable vascular infusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae5e7c82eac52c671b58538f8a1cb813 and manufactured by PEROUSE MEDICAL. The authorized representative in Taiwan is AMED CO., LTD..
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