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"Telifiano" percutaneous guide sheath set - Taiwan Registration ca737a9a755bda08b9d81ab5142a192a

Access comprehensive regulatory information for "Telifiano" percutaneous guide sheath set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca737a9a755bda08b9d81ab5142a192a 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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ca737a9a755bda08b9d81ab5142a192a
Registration Details
Taiwan FDA Registration: ca737a9a755bda08b9d81ab5142a192a
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Device Details

"Telifiano" percutaneous guide sheath set
TW: "ๆณฐๅˆฉ็ฆไบž่ซพ"็ถ“็šฎๅฐŽๅผ•้ž˜ๅฅ—็ต„
Risk Class 2

Registration Details

ca737a9a755bda08b9d81ab5142a192a

DHA05603077708

Product Details

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

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

Contract manufacturing;; input

Dates and Status

Mar 20, 2018

Mar 20, 2023

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