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"Medtronic" single-hole venous cannula - Taiwan Registration 0f41461e43c63088c7a1a24bdb0bfaa3

Access comprehensive regulatory information for "Medtronic" single-hole 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 0f41461e43c63088c7a1a24bdb0bfaa3 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.

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0f41461e43c63088c7a1a24bdb0bfaa3
Registration Details
Taiwan FDA Registration: 0f41461e43c63088c7a1a24bdb0bfaa3
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Device Details

"Medtronic" single-hole venous cannula
TW: "็พŽๆ•ฆๅŠ›" ๅ–ฎๅญ”ๅž‹้œ่„ˆๅฅ—็ฎก
Risk Class 2

Registration Details

0f41461e43c63088c7a1a24bdb0bfaa3

DHA00601003501

Company Information

Product Details

E Cardiovascular Medicine Science

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

import

Dates and Status

Aug 19, 2002

Aug 19, 2027