"Mykewei" cardiopulmonary vascular bypass auxiliary equipment (unsterilized) - Taiwan Registration 327b14c5e35571c2760d2c154261ab7e
Access comprehensive regulatory information for "Mykewei" cardiopulmonary vascular bypass auxiliary equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 327b14c5e35571c2760d2c154261ab7e and manufactured by MAQUET CARDIOPULMONARY AG. 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
Product Details
Limited to the first level recognition range of medical equipment management measures cardiopulmonary vascular bypass auxiliary equipment (E.4200).
E Cardiovascular Medicine Science
E.4200 ๅฟ่บ่ก็ฎก็น้่ก่ผๅฉ่จญๅ
import
Dates and Status
Dec 09, 2008
Dec 09, 2018
Jun 16, 2022
Cancellation Information
Logged out
่ช่ก้ตๅ ฅ