Taiwan FDA registration 327b14c5e35571c2760d2c154261ab7e
"Mykewei" cardiopulmonary vascular bypass auxiliary equipment (unsterilized)
TW: “邁柯唯”心肺血管繞道術輔助設備 (未滅菌)
Taiwan·Risk Class 1·MAQUET CARDIOPULMONARY AG·Registered Dec 09, 2008 – Dec 09, 2018CancelledRegistration details
- Analysis ID
- 327b14c5e35571c2760d2c154261ab7e
- Customs Code
- DHA04400730001
Company information
- Manufacturer
- MAQUET CARDIOPULMONARY AG
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN 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
- Dec 09, 2008
- Expiry Date
- Dec 09, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Mykewei" cardiopulmonary vascular bypass auxiliary equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 327b14c5e35571c2760d2c154261ab7e and manufactured by MAQUET CARDIOPULMONARY AG. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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