Pure Global

“Thoratec” CentriMag Cannula Kits - Taiwan Registration b568b9e8d58713a04088dd47375749b3

Access comprehensive regulatory information for “Thoratec” CentriMag Cannula Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b568b9e8d58713a04088dd47375749b3 and manufactured by Thoratec Switzerland GmbH. The authorized representative in Taiwan is Abbott Medical Taiwan 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
b568b9e8d58713a04088dd47375749b3
Registration Details
Taiwan FDA Registration: b568b9e8d58713a04088dd47375749b3
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Thoratec” CentriMag Cannula Kits
TW: “索羅格”善翠美血液套管組
Risk Class 2
MD

Registration Details

b568b9e8d58713a04088dd47375749b3

Ministry of Health Medical Device Import No. 030714

DHA05603071400

Company Information

Switzerland

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

Jan 24, 2018

Jan 24, 2028