Taiwan FDA registration be53577d14a4d1b6f92e177c485a6986

"Telifiano" Single lumen central venous catheter

TW: “泰利福亞諾” 單腔中央靜脈導管
Taiwan flagTaiwan·Risk Class 2·Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)·Registered Apr 16, 2018 – Apr 16, 2023Expired
Registration details
Analysis ID
be53577d14a4d1b6f92e177c485a6986
Customs Code
DHA05603080401
Company information
Manufacturer Country
United States;;Czechia
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1200 診斷用血管內導管
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Apr 16, 2018
Expiry Date
Apr 16, 2023
About this record

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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