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"Bayerdenick" implantable intracardiac defibrillator lead - Taiwan Registration c9b6c07e2add8fbd3a1d05d156512232

Access comprehensive regulatory information for "Bayerdenick" implantable intracardiac defibrillator lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c9b6c07e2add8fbd3a1d05d156512232 and manufactured by BIOTRONIC SE & CO. KG. The authorized representative in Taiwan is PRO PHARMA TAIWAN INC..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BIOTRONIC SE & CO. KG, BIOTRONIK SE & CO. KG, and 2 recent registrations in the same category. 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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c9b6c07e2add8fbd3a1d05d156512232
Registration Details
Taiwan FDA Registration: c9b6c07e2add8fbd3a1d05d156512232
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Device Details

"Bayerdenick" implantable intracardiac defibrillator lead
TW: "ๆ‹œ่€ณๅพทๅฐผๅ…‹"ๆคๅ…ฅๅผๅฟƒๅ…ง้™ค้กซๅ™จๅฐŽ็ทš
Risk Class 3
Cancelled

Registration Details

c9b6c07e2add8fbd3a1d05d156512232

DHA00601693206

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

E.3680 ๅฟƒ่ก€็ฎก็”จๆฐธไน…ๆˆ–ๆšซๆ™‚ๆ€งไน‹ๅฟƒๅพ‹่ชฟ็ฏ€ๅ™จ้›ปๆฅต

import

Dates and Status

Jul 28, 2006

Jul 28, 2011

Oct 30, 2012

Cancellation Information

Logged out

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