Taiwan FDA registration fca82564b816b37689f216f2fd9f90be

"Bayerdenix" implantable cardiac rhythm planning monitoring system

TW: “拜耳德尼克” 植入式心臟節律器規劃監視系統
Taiwan flagTaiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered May 14, 2008 – May 14, 2013Cancelled
Registration details
Analysis ID
fca82564b816b37689f216f2fd9f90be
Customs Code
DHA00601885501
Company information
Manufacturer Country
Germany
Authorized Representative
PRO PHARMA TAIWAN INC.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Import Information
import
Dates and status
Registration Date
May 14, 2008
Expiry Date
May 14, 2013
Cancellation Date
Jun 17, 2015
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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