Taiwan FDA registration ed8caeae5e14c5840b881561fc436eac

"Telifano" 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 Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated)·Registered May 02, 2018 – May 02, 2023Expired
Registration details
Analysis ID
ed8caeae5e14c5840b881561fc436eac
Customs Code
DHA05603088804
Company information
Manufacturer Country
Mexico;;United States
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)
J General hospital and personal use equipment
Product Type (Level 2)
J.5200 Endovascular catheters
Import Information
import
Dates and status
Registration Date
May 02, 2018
Expiry Date
May 02, 2023
About this record

Access comprehensive regulatory information for "Telifano" 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 ed8caeae5e14c5840b881561fc436eac 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..

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