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Onepais percutaneous puncture of the coronary artery dilation catheter - Taiwan Registration 5ed018b238482c33005241c5cbbebf92

Access comprehensive regulatory information for Onepais percutaneous puncture of the coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 5ed018b238482c33005241c5cbbebf92 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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5ed018b238482c33005241c5cbbebf92
Registration Details
Taiwan FDA Registration: 5ed018b238482c33005241c5cbbebf92
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Device Details

Onepais percutaneous puncture of the coronary artery dilation catheter
TW: ๆญๅฐผๆดพๅธ็ถ“็šฎ็ฉฟๅˆบๅ† ็‹€ๅ‹•่„ˆๆ“ดๅผตๅฐŽ็ฎก
Cancelled

Registration Details

5ed018b238482c33005241c5cbbebf92

DHA00600893200

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Nov 18, 1998

Nov 18, 2003

Jul 20, 2007

Cancellation Information

Logged out

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