Taiwan FDA registration 314c949136501449a8a1519870adc9fb
"McVier" Ayer microporous membrane oxygenator (with Bioline coating)
TW: “邁柯唯”艾爾微孔膜氧合器(含Bioline塗層)
Taiwan·Risk Class 2·Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH·Registered Jul 02, 2012 – Jul 02, 2022CancelledRegistration details
- Analysis ID
- 314c949136501449a8a1519870adc9fb
- Customs Code
- DHA00602374600
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
- Jul 02, 2012
- Expiry Date
- Jul 02, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "McVier" Ayer microporous 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 314c949136501449a8a1519870adc9fb and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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