Taiwan FDA registration 21a444a898189e73d6d7f75edfff4b43

"Bayerdenik" Kolo implantable bipolar center wire

TW: “拜耳德尼克”可洛植入式雙極心導線
Taiwan flagTaiwan·Risk Class 3·BIOTRONIC SE & CO. KG·Registered Jun 14, 2012 – Jun 14, 2017Cancelled
Registration details
Analysis ID
21a444a898189e73d6d7f75edfff4b43
Customs Code
DHA00602372801
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
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
Dates and status
Registration Date
Jun 14, 2012
Expiry Date
Jun 14, 2017
Cancellation Date
Oct 25, 2013
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Bayerdenik" Kolo implantable bipolar center wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 21a444a898189e73d6d7f75edfff4b43 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 BIOTRONIC SE & 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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