Taiwan FDA registration 22c54e83fc858c556d015d1edba0862f
"Mikevi" diffusion membrane oxygenator (with Bioline coating)
TW: “邁柯唯”擴散膜氧合器(含Bioline塗層)
Taiwan·Risk Class 2·Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH·Registered Mar 31, 2011 – Mar 31, 2026CancelledRegistration details
- Analysis ID
- 22c54e83fc858c556d015d1edba0862f
- Customs Code
- DHA00602211002
Company information
- Manufacturer Country
- Germany
- 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.4350 Cardiopulmonary vascular bypass and oxygen apparatus
- Import Information
- import
Dates and status
- Registration Date
- Mar 31, 2011
- Expiry Date
- Mar 31, 2026
- Cancellation Date
- Jun 27, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Mikevi" diffusion membrane oxygenator (with Bioline coating) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22c54e83fc858c556d015d1edba0862f and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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