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"Caudix" guide tube - Taiwan Registration 30d4d95939063e7c6cebb2af559ae7ae

Access comprehensive regulatory information for "Caudix" guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30d4d95939063e7c6cebb2af559ae7ae and manufactured by Cordis US Corp.;; Cardinal Health Mexico 244 S. de R.L. de C.V.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CORDIS CORPORATION, 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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30d4d95939063e7c6cebb2af559ae7ae
Registration Details
Taiwan FDA Registration: 30d4d95939063e7c6cebb2af559ae7ae
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Device Details

"Caudix" guide tube
TW: "่€ƒ่ฟชๆ–ฏ" ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2

Registration Details

30d4d95939063e7c6cebb2af559ae7ae

DHA00600864201

Company Information

Product Details

Vacuum.

0607 Cardiac catheterization

import

Dates and Status

Mar 22, 2023

Apr 20, 2028

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