"Ikefu" rapid hemoglobin correction control assay set group - Taiwan Registration 759dc18fa5005337a8b42446eb968235
Access comprehensive regulatory information for "Ikefu" rapid hemoglobin correction control assay set group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 759dc18fa5005337a8b42446eb968235 and manufactured by EKF-DIAGNOSTIC GMBH. The authorized representative in Taiwan is Y.H. BIOTEK 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
ๅจไฝฟ็จHemo_Controlๅ ๅบฆ่จๅๆฐๆธฌๅฎไนๅ,็จไปฅๆธฌๅฎ็ฎๆจๆธๅผ.
A Clinical chemistry and clinical toxicology
A.1660 Quality control materials (analytical and non-analytical)
import
Dates and Status
Apr 11, 2006
Apr 11, 2016
Jun 28, 2018
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ