Kepifibrinogen assay reagent - Taiwan Registration 07449902c14eb9b704f19d3932e07f99
Access comprehensive regulatory information for Kepifibrinogen assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07449902c14eb9b704f19d3932e07f99 and manufactured by SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT. The authorized representative in Taiwan is KUO'S YUAN IN 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
ๆชขๆธฌ่กๆผฟไธญ็็บ็ถญ่็ฝๅ(Fibrinogen).
B Hematology, pathology, and genetics
B.7340 Fibrinogen Confirmation System
import
Dates and Status
May 20, 2013
May 20, 2018
Nov 04, 2019
Cancellation Information
Logged out
ๆชๅฑๅปถ่้พๆ่