Taiwan FDA registration f55edf0dc548bc0c5b085d48c9dfc5b1

"Meikewei" cardiopulmonary cardiopulmonary bypass tubing group

TW: “邁柯唯”心肺體外循環管路組
Taiwan flagTaiwan·Risk Class 2·MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; Maquet Cardiopulmonary GmbH·Registered Oct 07, 2009 – Oct 07, 2019Cancelled
Registration details
Analysis ID
f55edf0dc548bc0c5b085d48c9dfc5b1
Customs Code
DHA00602022904
Company information
Manufacturer Country
Türkiye;;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 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
Import Information
import
Dates and status
Registration Date
Oct 07, 2009
Expiry Date
Oct 07, 2019
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for "Meikewei" cardiopulmonary cardiopulmonary bypass tubing group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f55edf0dc548bc0c5b085d48c9dfc5b1 and manufactured by MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; Maquet Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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