Taiwan FDA registration 57bf4d5748a7abbc37fac3673ab1935c
"Meikowei" is an artificial blood vessel at the root of the aorta
TW: “邁柯唯”英特佳主動脈根部人工血管
Taiwan·Risk Class 2·INTERVASCULAR SAS·Registered Jul 24, 2012 – Jul 24, 2027ActiveRegistration details
- Analysis ID
- 57bf4d5748a7abbc37fac3673ab1935c
- Customs Code
- DHA00602390507
Company information
- Manufacturer
- INTERVASCULAR SAS
- Manufacturer Country
- France
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3450 血管移植彌補物
- Import Information
- import
Dates and status
- Registration Date
- Jul 24, 2012
- Expiry Date
- Jul 24, 2027
About this record
Access comprehensive regulatory information for "Meikowei" is an artificial blood vessel at the root of the aorta in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57bf4d5748a7abbc37fac3673ab1935c and manufactured by INTERVASCULAR SAS. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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