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"Telifiano" ductus arteriosus sleeve - Taiwan Registration 4a125f8cce91f5446e341153ba137b18

Access comprehensive regulatory information for "Telifiano" 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 4a125f8cce91f5446e341153ba137b18 and manufactured by Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), 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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4a125f8cce91f5446e341153ba137b18
Registration Details
Taiwan FDA Registration: 4a125f8cce91f5446e341153ba137b18
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Device Details

"Telifiano" ductus arteriosus sleeve
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ๅ‹•่„ˆๅฐŽ็ฎกๅฅ—็ต„
Risk Class 2

Registration Details

4a125f8cce91f5446e341153ba137b18

DHA05603064007

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Contract manufacturing;; input

Dates and Status

Jan 02, 2018

Jan 02, 2028

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