"Bayerdenick" implantable intracardiac defibrillator lead
Taiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Jul 28, 2006 – Jul 28, 2011Cancelled- Analysis ID
- c9b6c07e2add8fbd3a1d05d156512232
- Customs Code
- DHA00601693206
- Manufacturer
- BIOTRONIC SE & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- PRO PHARMA TAIWAN INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3680 心血管用永久或暫時性之心律調節器電極
- Import Information
- import
- Registration Date
- Jul 28, 2006
- Expiry Date
- Jul 28, 2011
- Cancellation Date
- Oct 30, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.