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"Caudix" Akwaia T3 coronary artery dilation catheter - Taiwan Registration 008d6402e697708ad292161bc9d33d09

Access comprehensive regulatory information for "Caudix" Akwaia T3 coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 008d6402e697708ad292161bc9d33d09 and manufactured by CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

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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008d6402e697708ad292161bc9d33d09
Registration Details
Taiwan FDA Registration: 008d6402e697708ad292161bc9d33d09
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Device Details

"Caudix" Akwaia T3 coronary artery dilation catheter
TW: "่€ƒ่ฟชๆ–ฏ" ้˜ฟ่‘ตไบžT3ๅ† ็‹€ๅ‹•่„ˆๆ“ดๅผตๅฐŽ็ฎก
Cancelled

Registration Details

008d6402e697708ad292161bc9d33d09

DHA00601028100

Product Details

E Cardiovascular Medicine Science

import

Dates and Status

Apr 23, 2003

Apr 23, 2008

Nov 27, 2012

Cancellation Information

Logged out

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