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"Bayerdenix" implantable cardiac rhythm planning monitoring system - Taiwan Registration fca82564b816b37689f216f2fd9f90be

Access comprehensive regulatory information for "Bayerdenix" implantable cardiac rhythm planning monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fca82564b816b37689f216f2fd9f90be 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, 1 companies making similar products including BIOTRONIK GMBH & CO. KG, and 1 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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fca82564b816b37689f216f2fd9f90be
Registration Details
Taiwan FDA Registration: fca82564b816b37689f216f2fd9f90be
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Device Details

"Bayerdenix" implantable cardiac rhythm planning monitoring system
TW: โ€œๆ‹œ่€ณๅพทๅฐผๅ…‹โ€ ๆคๅ…ฅๅผๅฟƒ่‡Ÿ็ฏ€ๅพ‹ๅ™จ่ฆๅŠƒ็›ฃ่ฆ–็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

fca82564b816b37689f216f2fd9f90be

DHA00601885501

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

May 14, 2008

May 14, 2013

Jun 17, 2015

Cancellation Information

Logged out

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