"Bayerdenik" Setex implantable cardiac synchronization therapy heart rhythm regulator - Taiwan Registration 4899c56bf67f659702d35381e8991582
Access comprehensive regulatory information for "Bayerdenik" Setex implantable cardiac synchronization therapy heart rhythm regulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4899c56bf67f659702d35381e8991582 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order.
E Cardiovascular Medicine Science
E.3610 Pulsator of implantable cardiac rhythm apparatus
import
Dates and Status
Oct 29, 2007
Oct 29, 2017
Oct 25, 2013
Cancellation Information
Logged out
่ช่ซ่จป้ท