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"Telifiano" ductus arteriosus sleeve - Taiwan Registration 0efa1f11ef463ccbeb233a5613e2eca9

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 0efa1f11ef463ccbeb233a5613e2eca9 and manufactured by Arrow Internacional de Chihuahua S.A. de C.V.;; 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 International C.R. a.s.;; 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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0efa1f11ef463ccbeb233a5613e2eca9
Registration Details
Taiwan FDA Registration: 0efa1f11ef463ccbeb233a5613e2eca9
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Device Details

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

Registration Details

0efa1f11ef463ccbeb233a5613e2eca9

DHA05603063807

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

Jan 02, 2018

Jan 02, 2028

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