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Arterial cannula - Taiwan Registration 71ffc41106477bbe46eef6af0a818260

Access comprehensive regulatory information for Arterial cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71ffc41106477bbe46eef6af0a818260 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, 4 companies making similar products including Medtronic Perfusion Systems;; Medtronic Inc., MEDTRONIC CARDIAC SURGICAL PRODUCTS, and 5 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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71ffc41106477bbe46eef6af0a818260
Registration Details
Taiwan FDA Registration: 71ffc41106477bbe46eef6af0a818260
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Device Details

Arterial cannula
TW: ๅ‹•่„ˆๅฅ—็ฎก
Risk Class 2

Registration Details

71ffc41106477bbe46eef6af0a818260

DHA00600891102

Company Information

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Oct 31, 1998

Oct 31, 2028