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"Telifiano" Single lumen central venous catheter - Taiwan Registration be53577d14a4d1b6f92e177c485a6986

Access comprehensive regulatory information for "Telifiano" Single lumen central venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be53577d14a4d1b6f92e177c485a6986 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..

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be53577d14a4d1b6f92e177c485a6986
Registration Details
Taiwan FDA Registration: be53577d14a4d1b6f92e177c485a6986
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Device Details

"Telifiano" Single lumen central venous catheter
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ ๅ–ฎ่…”ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

be53577d14a4d1b6f92e177c485a6986

DHA05603080401

Product Details

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

E Cardiovascular Medicine Science

E.1200 ่จบๆ–ท็”จ่ก€็ฎกๅ…งๅฐŽ็ฎก

Input;; Contract manufacturing

Dates and Status

Apr 16, 2018

Apr 16, 2023