Taiwan FDA registration 4deb5d84763543ca6e093f89c948d2ab

"McCovi" centrifugal pump (including Bioline)

TW: “邁柯唯”離心幫浦(含Bioline)

Taiwan·Risk Class 3·Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH·Registered May 04, 2010 – May 04, 2025Expired

Registration details

Analysis ID: 4deb5d84763543ca6e093f89c948d2ab
Customs Code: DHA00602099009

Company information

Manufacturer: Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH
Manufacturer Country: Germany
Authorized Representative: GETINGE GROUP TAIWAN CO., LTD.

Product details

Intended Use: Centrifugal pumps are used in artificial cardiopulmonary support systems during surgery, or cardiopulmonary bypass. Centrifugal pumps deliver blood within a defined flow range.
Product Type (Level 1): E Cardiovascular Medicine Science
Import Information: import

Dates and status

Registration Date: May 04, 2010
Expiry Date: May 04, 2025

About this record

Access comprehensive regulatory information for "McCovi" centrifugal pump (including Bioline) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4deb5d84763543ca6e093f89c948d2ab and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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