Taiwan FDA registration 5a2717752125261b6da2b78d00f79d5e
"Serucun" percutaneous intravascular angioplasty balloon catheter
TW: “瑟璐潯”經皮血管內血管成形術球囊導管
Taiwan·Risk Class 2·M.A. Med Alliance SA;; MedAlliance LLC·Registered Feb 21, 2023 – Feb 21, 2028ActiveRegistration details
- Analysis ID
- 5a2717752125261b6da2b78d00f79d5e
- Customs Code
- DHA05603599504
Company information
- Manufacturer
- M.A. Med Alliance SA;; MedAlliance LLC
- Manufacturer Country
- United States;;Switzerland
- Authorized Representative
- REGISTAR CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Feb 21, 2023
- Expiry Date
- Feb 21, 2028
About this record
Access comprehensive regulatory information for "Serucun" percutaneous intravascular angioplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a2717752125261b6da2b78d00f79d5e and manufactured by M.A. Med Alliance SA;; MedAlliance LLC. The authorized representative in Taiwan is REGISTAR CO., LTD..
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