"Bayerson" kinetic source line coronary balloon dilation catheter - Taiwan Registration 0a41c90615c06be99912d0c51e047e1f
Access comprehensive regulatory information for "Bayerson" kinetic source line coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0a41c90615c06be99912d0c51e047e1f and manufactured by BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., LTD..
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.0005.
import
Dates and Status
Feb 19, 2009
Feb 19, 2014
Nov 15, 2016
Cancellation Information
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