Taiwan FDA registration 5283e46985a67b7da0eca4bfedf3dc40

"Arno" multi-lumen hemodialysis catheter

TW: “亞諾”多腔式血液透析導管
Taiwan flagTaiwan·Risk Class 2·Arrow International, Inc;; Arrow Internacional de Chihuahua S.A. de C.V.·Registered Nov 16, 2016 – Nov 16, 2021Cancelled
Registration details
Analysis ID
5283e46985a67b7da0eca4bfedf3dc40
Customs Code
DHA05602905203
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)
H Gastroenterology and urology
Product Type (Level 2)
H.5540 Blood Access Devices and Accessories
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Nov 16, 2016
Expiry Date
Nov 16, 2021
Cancellation Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Arno" multi-lumen hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5283e46985a67b7da0eca4bfedf3dc40 and manufactured by Arrow International, Inc;; Arrow Internacional de Chihuahua S.A. de C.V.. 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 LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s., 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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