Taiwan FDA registration ce9cbe49f2d4924736b7f26de882b20b
"Meidus" cardiopulmonary vascular bypass aid device (unsterilized)
TW: "美德思" 心肺血管繞道術輔助設備 (未滅菌)
Taiwan·Risk Class 1·MEDOS MEDIZINTECHNIK AG·Registered May 01, 2013 – May 01, 2023ExpiredRegistration details
- Analysis ID
- ce9cbe49f2d4924736b7f26de882b20b
- Customs Code
- DHA04401295900
Company information
- Manufacturer
- MEDOS MEDIZINTECHNIK AG
- Manufacturer Country
- Germany
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures cardiopulmonary vascular bypass auxiliary equipment (E.4200).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4200 心肺血管繞道術輔助設備
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2013
- Expiry Date
- May 01, 2023
About this record
Access comprehensive regulatory information for "Meidus" cardiopulmonary vascular bypass aid device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce9cbe49f2d4924736b7f26de882b20b and manufactured by MEDOS MEDIZINTECHNIK AG. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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