Remai dysentery amoeba test panel - Taiwan Registration 9b330dcca0795217d364ae60b17d35ad
Access comprehensive regulatory information for Remai dysentery amoeba test panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b330dcca0795217d364ae60b17d35ad and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is Qixin Biotechnology 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
็จๆผๅฎๆงๅตๆธฌไบบ้ก็ณไพฟไน่ๅๆถฒไธญไน็ข็พ้ฟ็ฑณๅทดๅฐไธๆงๆๅ(Entamoeba histolytica specific antigen, EHSA).
C Immunology and microbiology
C.3220 ็ข็พ้ฟ็ฑณๅทด่กๆธ ่ฉฆๅ
import
Dates and Status
Apr 28, 2006
Apr 28, 2011
Nov 08, 2012
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ

