"Meikewei" cardiopulmonary cardiopulmonary bypass tubing group - Taiwan Registration f55edf0dc548bc0c5b085d48c9dfc5b1
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..
This page provides complete technical specifications, regulatory compliance details. 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.
Device Details
Registration Details
f55edf0dc548bc0c5b085d48c9dfc5b1
DHA00602022904
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
import
Dates and Status
Oct 07, 2009
Oct 07, 2019
Jun 16, 2022
Cancellation Information
Logged out
่ช่ก้ตๅ ฅ

