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"Caudix" Durising coronary artery dilation duct - Taiwan Registration bf79cfc2d04840d3054904468b5e04f5

Access comprehensive regulatory information for "Caudix" Durising coronary artery dilation duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bf79cfc2d04840d3054904468b5e04f5 and manufactured by CORDIS CASHEL. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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bf79cfc2d04840d3054904468b5e04f5
Registration Details
Taiwan FDA Registration: bf79cfc2d04840d3054904468b5e04f5
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Device Details

"Caudix" Durising coronary artery dilation duct
TW: โ€œ่€ƒ่ฟชๆ–ฏโ€ ๆœ่Šฎๆ˜Ÿๅ† ็‹€ๅ‹•่„ˆๆ“ดๅผตๅฐŽ็ฎก
Risk Class 3
Cancelled

Registration Details

bf79cfc2d04840d3054904468b5e04f5

DHA00601914409

Company Information

Ireland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.0005.

import

Dates and Status

Jul 31, 2008

Jul 31, 2018

Jul 15, 2022

Cancellation Information

Logged out

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