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"Caudix" guide tube - Taiwan Registration 933bb9afe544a2813ab70de656780564

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 933bb9afe544a2813ab70de656780564 and manufactured by CORDIS CORPORATION. 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 US Corp.;; Cardinal Health Mexico 244 S. de R.L. de C.V., 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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933bb9afe544a2813ab70de656780564
Registration Details
Taiwan FDA Registration: 933bb9afe544a2813ab70de656780564
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Device Details

"Caudix" guide tube
TW: โ€œ่€ƒ่ฟชๆ–ฏโ€ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2

Registration Details

933bb9afe544a2813ab70de656780564

DHA00602294300

Company Information

United States

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 29, 2011

Nov 29, 2026

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