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"Arno" ductus arteriosus group - Taiwan Registration 6b3238d92b50aa7997b883cc39fced3b

Access comprehensive regulatory information for "Arno" ductus arteriosus group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b3238d92b50aa7997b883cc39fced3b and manufactured by Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International CR, a.s.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), ARROW INTERNATIONAL INC., and 3 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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6b3238d92b50aa7997b883cc39fced3b
Registration Details
Taiwan FDA Registration: 6b3238d92b50aa7997b883cc39fced3b
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Device Details

"Arno" ductus arteriosus group
TW: โ€œไบž่ซพโ€ๅ‹•่„ˆๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

6b3238d92b50aa7997b883cc39fced3b

DHA05602643902

Company Information

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 18, 2014

Aug 18, 2024