Taiwan FDA registration 1ce7a43e6c77fa76fb8bb59751f09c00

"Mekewei" cardiopulmonary bypass tubing set (with Bioline coating)

TW: “邁柯唯”體外循環管路組(含Bioline塗層)

Taiwan·Risk Class 3·Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH·Registered May 18, 2011 – May 18, 2026Expired

Registration details

Analysis ID: 1ce7a43e6c77fa76fb8bb59751f09c00
Customs Code: DHA00602231507

Company information

Manufacturer: Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH
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.4210 心肺血管繞道術之血管導管、套管及管子;; E.4350 心肺血管繞道術和氧器;; E.4360 非滾筒式心肺血管繞道術血液循環幫浦
Import Information: import

Dates and status

Registration Date: May 18, 2011
Expiry Date: May 18, 2026

About this record

Access comprehensive regulatory information for "Mekewei" cardiopulmonary bypass tubing set (with Bioline coating) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1ce7a43e6c77fa76fb8bb59751f09c00 and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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