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"Caudix" supersonic dilated vascular stents - Taiwan Registration dd2b556d8654a0f64b670585468b0abf

Access comprehensive regulatory information for "Caudix" supersonic dilated vascular stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dd2b556d8654a0f64b670585468b0abf and manufactured by CORDIS CASHEL. 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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dd2b556d8654a0f64b670585468b0abf
Registration Details
Taiwan FDA Registration: dd2b556d8654a0f64b670585468b0abf
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Device Details

"Caudix" supersonic dilated vascular stents
TW: "่€ƒ่ฟชๆ–ฏ" ่ถ…้Ÿณ้€Ÿๆ“ดๅผตๅผ่ก€็ฎกๆ”ฏๆžถ
Risk Class 3
Cancelled

Registration Details

dd2b556d8654a0f64b670585468b0abf

DHA00600982501

Company Information

Product Details

E Cardiovascular Medicine Science

import

Dates and Status

Feb 15, 2002

Feb 15, 2017

Nov 15, 2019

Cancellation Information

Logged out

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