Taiwan FDA registration bf11caaa7f734e437c80bf72c2db7a82

"Arno" multi-lumen central venous catheter group

TW: “亞諾”多腔中央靜脈導管組
Taiwan flagTaiwan·Risk Class 2·Arrow International LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s.·Registered Mar 20, 2022 – Mar 20, 2027Active
Registration details
Analysis ID
bf11caaa7f734e437c80bf72c2db7a82
Customs Code
DHA05603533501
Company information
Manufacturer Country
United States;;Czechia
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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
Mar 20, 2022
Expiry Date
Mar 20, 2027
About this record

Access comprehensive regulatory information for "Arno" multi-lumen central venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf11caaa7f734e437c80bf72c2db7a82 and manufactured by Arrow International LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices