Pure Global

"Medtronic" double-foramen venous cannula - Taiwan Registration 58f16fa8f3bc67c6c578824e762a149d

Access comprehensive regulatory information for "Medtronic" double-foramen venous cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58f16fa8f3bc67c6c578824e762a149d and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
58f16fa8f3bc67c6c578824e762a149d
Registration Details
Taiwan FDA Registration: 58f16fa8f3bc67c6c578824e762a149d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" double-foramen venous cannula
TW: "็พŽๆ•ฆๅŠ›" ้›™ๅญ”้œ่„ˆๅฅ—็ฎก
Risk Class 2

Registration Details

58f16fa8f3bc67c6c578824e762a149d

DHA00601002801

Company Information

Product Details

Vacuum.

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

Aug 15, 2002

Aug 15, 2027