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"Bayer Dennick" Kent intracardiac defibrillator lead - Taiwan Registration bda1554e53fdc32342eac323f9b463d0

Access comprehensive regulatory information for "Bayer Dennick" Kent 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 bda1554e53fdc32342eac323f9b463d0 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. 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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bda1554e53fdc32342eac323f9b463d0
Registration Details
Taiwan FDA Registration: bda1554e53fdc32342eac323f9b463d0
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Device Details

"Bayer Dennick" Kent intracardiac defibrillator lead
TW: โ€œๆ‹œ่€ณๅพทๅฐผๅ…‹โ€่‚ฏ็‰นๅฟƒๅ…ง้™ค้กซๅ™จๅฐŽ็ทš
Risk Class 3
Cancelled

Registration Details

bda1554e53fdc32342eac323f9b463d0

DHA00601799509

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

Apr 10, 2007

Apr 10, 2012

May 05, 2014

Cancellation Information

Logged out

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