AndoCor Pericardial Sump - Taiwan Registration 8212e4e351375d3dc98725cfd2893f6c
Access comprehensive regulatory information for AndoCor Pericardial Sump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8212e4e351375d3dc98725cfd2893f6c and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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
8212e4e351375d3dc98725cfd2893f6c
Ministry of Health Medical Device Import No. 031877
DHA05603187704
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular devices
E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass
Imported from abroad
Dates and Status
Dec 22, 2018
Dec 22, 2023