Taiwan FDA registration 6dc069ebbfc2de66f2dcb2852ad087df

"Arno" percutaneous guide sheath group

TW: “亞諾”經皮導引鞘組
Taiwan flagTaiwan·Risk Class 2·Arrow Internacional de Chihuahua S.A. de C.V.;; ARROW INTERNATIONAL INC.·Registered Aug 02, 2016 – Aug 02, 2026Active
Registration details
Analysis ID
6dc069ebbfc2de66f2dcb2852ad087df
Customs Code
DHA05602875101
Company information
Manufacturer Country
Mexico;;United States
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
Details as in the Chinese copy of the approved copy Application for change: change in efficacy, use or indications: detailed as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on March 1, 111 will be withdrawn and invalidated).
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1340 Catheter Introducers
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Aug 02, 2016
Expiry Date
Aug 02, 2026
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About this record

Access comprehensive regulatory information for "Arno" percutaneous guide sheath group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6dc069ebbfc2de66f2dcb2852ad087df and manufactured by Arrow Internacional de Chihuahua S.A. de C.V.;; ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ARROW INTERNATIONAL INC., Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International Cr, a.s., and 2 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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