Taiwan FDA registration 0efa1f11ef463ccbeb233a5613e2eca9

"Telifiano" ductus arteriosus sleeve

TW: “泰利福亞諾”動脈導管套組
Taiwan flagTaiwan·Risk Class 2·Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated)·Registered Jan 02, 2018 – Jan 02, 2028Active
Registration details
Analysis ID
0efa1f11ef463ccbeb233a5613e2eca9
Customs Code
DHA05603063807
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)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1250 Percutaneous catheters
Import Information
import
Dates and status
Registration Date
Jan 02, 2018
Expiry Date
Jan 02, 2028
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About this record

Access comprehensive regulatory information for "Telifiano" ductus arteriosus sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0efa1f11ef463ccbeb233a5613e2eca9 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..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated), 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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