"Arno" percutaneous guide sheath group - Taiwan Registration d08c7fc5edf538348cc48c8d9bfd8202
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 d08c7fc5edf538348cc48c8d9bfd8202 and manufactured by 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 Internacional de Chihuahua S.A. de C.V.;; 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
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.1340 Catheter Introducers
import
Dates and Status
Nov 02, 2010
Nov 02, 2020
Jun 07, 2022
Cancellation Information
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"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. (Subsidiary of Teleflex Inc.);; Arrow International Cr, a.s.
a34b4647c00dc7bede8b0a2c1573e4b1
2