Spiex cytoplasm separator cannula set - Taiwan Registration dc2ab4c93cac3c77595786e50c5cee6f

Access comprehensive regulatory information for Spiex cytoplasm separator cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc2ab4c93cac3c77595786e50c5cee6f and manufactured by BIOSAFE Ltd. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOSAFE Ltd, 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.