"Arno" percutaneous guide sheath group - Taiwan Registration a34b4647c00dc7bede8b0a2c1573e4b1
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 a34b4647c00dc7bede8b0a2c1573e4b1 and manufactured by Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International Cr, a.s.. 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 Internacional de Chihuahua S.A. de C.V.;; ARROW INTERNATIONAL INC., 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
a34b4647c00dc7bede8b0a2c1573e4b1
DHA05602638400
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Chinese instruction manual (the original label, instruction manual or packaging approved on March 1, 111 will be withdrawn and invalidated).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
import
Dates and Status
Jul 02, 2014
Jul 02, 2029
"Arno" percutaneous guide sheath group
Arrow Internacional de Chihuahua S.A. de C.V.;; ARROW INTERNATIONAL INC.
6dc069ebbfc2de66f2dcb2852ad087df
2
"Arno" percutaneous guide sheath group
ARROW INTERNATIONAL INC.
d08c7fc5edf538348cc48c8d9bfd8202
2