Vitex immunoassay group Toxoplasma antibody IgM reagent - Taiwan Registration 42a776077aea2401a2886c601dc495fc
Access comprehensive regulatory information for Vitex immunoassay group Toxoplasma antibody IgM reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42a776077aea2401a2886c601dc495fc and manufactured by ORTHO-CLINICAL DIAGNOSTICS. The authorized representative in Taiwan is DKSH TAIWAN 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
For in vitro qualitative detection of Toxoplasma gondii antibody IgM in human serum and plasma (heparin, EDTA, or sodium citrate).
A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
A.1150 ๆ กๆญฃๅ;; C.3780 ๅผๆผฟ่ฒ่กๆธ ่ฉฆๅ
import
Dates and Status
Feb 09, 2009
Feb 09, 2029

