“BIOTRONIK” Pulsar-18 Self Expanding Peripheral Stent System - Taiwan Registration 3b11509b0b896a7adfd85d4c4187bc76

Access comprehensive regulatory information for “BIOTRONIK” Pulsar-18 Self Expanding Peripheral Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b11509b0b896a7adfd85d4c4187bc76 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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.