“DIESSE” CHORUS TOXOPLASMA IgG - Taiwan Registration cb8b66c4937509758f6f39850539b64c
Access comprehensive regulatory information for “DIESSE” CHORUS TOXOPLASMA IgG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb8b66c4937509758f6f39850539b64c and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIESSE DIAGNOSTICA SENESE S.P.A., and 1 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
Registration Details
cb8b66c4937509758f6f39850539b64c
Ministry of Health Medical Device Import No. 027887
DHA05602788705
Product Details
This product is used with the Chorus system to quantitatively detect Toxoplasma IgG antibodies in human serum.
C Immunology and microbiology devices
C3780 Toxoplasma rodent serum reagent
Imported from abroad
Dates and Status
Oct 29, 2015
Oct 29, 2025

