"Arno" percutaneous guide sheath group - Taiwan Registration 6dc069ebbfc2de66f2dcb2852ad087df
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.
Device Details
Registration Details
6dc069ebbfc2de66f2dcb2852ad087df
DHA05602875101
Product Details
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Chinese instruction manual (the original label, instruction manual or packaging approved on March 1, 111 will be withdrawn and invalidated).
E Cardiovascular Medicine Science
E.1340 Catheter Introducers
Contract manufacturing;; input
Dates and Status
Aug 02, 2016
Aug 02, 2026
"Arno" percutaneous guide sheath group
Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International Cr, a.s.
a34b4647c00dc7bede8b0a2c1573e4b1
2
"Arno" percutaneous guide sheath group
ARROW INTERNATIONAL INC.
d08c7fc5edf538348cc48c8d9bfd8202
2