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"Medtronic" pediatric cannula with arterial root - Taiwan Registration 212ea7e83ab5b139470dc9915054b3ae

Access comprehensive regulatory information for "Medtronic" pediatric cannula with arterial root in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 212ea7e83ab5b139470dc9915054b3ae 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, 1 companies making similar products including MEDTRONIC PERFUSION SYSTEMS, and 1 recent registrations in the same category. 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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212ea7e83ab5b139470dc9915054b3ae
Registration Details
Taiwan FDA Registration: 212ea7e83ab5b139470dc9915054b3ae
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Device Details

"Medtronic" pediatric cannula with arterial root
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅฐๅ…’็”จๅ‹•่„ˆๆ น้ƒจๅฅ—็ฎก
Risk Class 2

Registration Details

212ea7e83ab5b139470dc9915054b3ae

DHA00601952508

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

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

import

Dates and Status

Dec 24, 2008

Dec 24, 2028

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