Taiwan FDA registration 6efb4c5e9b122f34846c55113bebffcb
"Plusrite" ultrasound guidance for a complete set of implantable vascular infusion
TW: “普羅斯”超音波引導用全套式植入式血管輸注器
Taiwan·Risk Class 2·PEROUSE MEDICAL·Registered Feb 24, 2014 – Feb 24, 2029ActiveRegistration details
- Analysis ID
- 6efb4c5e9b122f34846c55113bebffcb
- Customs Code
- DHA05602582206
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
- Product Type (Level 2)
- J.5965 Subcutaneous implantable intravascular injection port and guide
- Import Information
- import
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2029
About this record
Access comprehensive regulatory information for "Plusrite" 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 6efb4c5e9b122f34846c55113bebffcb and manufactured by PEROUSE MEDICAL. The authorized representative in Taiwan is AMED CO., LTD..
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