Taiwan FDA registration 32674156d1a8298ba3542e519fe825d9
Xenios console
TW: 賽耐司血液幫浦系統
Taiwan·Risk Class 2·MD·Xenios AG·Registered Jul 05, 2017 – Jul 05, 2027ActiveRegistration details
- Analysis ID
- 32674156d1a8298ba3542e519fe825d9
- License Form
- Ministry of Health Medical Device Import No. 029953
- Customs Code
- DHA05602995302
Company information
- Manufacturer
- Xenios AG
- Manufacturer Country
- Germany
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4220 Cardiopulmonary machine for cardiopulmonary vascular bypass
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 05, 2017
- Expiry Date
- Jul 05, 2027
About this record
Access comprehensive regulatory information for Xenios console in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 32674156d1a8298ba3542e519fe825d9 and manufactured by Xenios AG. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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