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"Byrdnik" quick exchange coronary stent system - Taiwan Registration 3d3ce67ef16a0fd9e43985f4afc3eadd

Access comprehensive regulatory information for "Byrdnik" quick exchange coronary stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3d3ce67ef16a0fd9e43985f4afc3eadd and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..

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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3d3ce67ef16a0fd9e43985f4afc3eadd
Registration Details
Taiwan FDA Registration: 3d3ce67ef16a0fd9e43985f4afc3eadd
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Device Details

"Byrdnik" quick exchange coronary stent system
TW: โ€œๆ‹œ็ˆพๅพทๅฐผๅ…‹โ€ๅฟซ้€Ÿไบคๆ›ๅ† ็‹€ๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

3d3ce67ef16a0fd9e43985f4afc3eadd

DHA00601884903

Company Information

Switzerland

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

May 09, 2008

May 09, 2013

Jun 17, 2015

Cancellation Information

Logged out

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