"Meikewei" microporous membrane oxygenator
Taiwan·Risk Class 2·Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH·Registered Sep 25, 2009 – Sep 25, 2024Cancelled- Analysis ID
- 9c2268b23b75b7c829fd08e7e226610a
- Customs Code
- DHA00602020006
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
- 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
- Registration Date
- Sep 25, 2009
- Expiry Date
- Sep 25, 2024
- Cancellation Date
- Jun 27, 2023
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for "Meikewei" microporous membrane oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c2268b23b75b7c829fd08e7e226610a and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH, and 3 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.