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"Arno" ductus arteriosus sleeve - Taiwan Registration f1823b6ffb7935ae1f3d4e6f5624d640

Access comprehensive regulatory information for "Arno" ductus arteriosus sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f1823b6ffb7935ae1f3d4e6f5624d640 and manufactured by Arrow International LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s.. The authorized representative in Taiwan is TELEFLEX MEDICAL 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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f1823b6ffb7935ae1f3d4e6f5624d640
Registration Details
Taiwan FDA Registration: f1823b6ffb7935ae1f3d4e6f5624d640
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Device Details

"Arno" ductus arteriosus sleeve
TW: โ€œไบž่ซพโ€ๅ‹•่„ˆๅฐŽ็ฎกๅฅ—็ต„
Risk Class 2

Registration Details

f1823b6ffb7935ae1f3d4e6f5624d640

DHA05603390404

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Aug 26, 2020

Aug 26, 2025