Spiex cytoplasm separator cannula set - Taiwan Registration 60a2dc7ccd625887c89c1aa28c1d9866
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 60a2dc7ccd625887c89c1aa28c1d9866 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
B Hematology, pathology, and genetics
B.9100 Containers for the collection and disposal of blood and blood components
import
Dates and Status
May 10, 2013
May 10, 2028