Qualitative Toxoplasma gondii Test Kit - Vietnam Registration 2400620ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Qualitative Toxoplasma gondii Test Kit in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2400620ĐKLH/BYT-HTTB and manufactured by Sacace Biotechnologies S.r.l. The authorized representative in Vietnam is CÔNG TY TNHH THIẾT BỊ KHOA HỌC KỸ THUẬT VIỆT HUY.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
2400620ĐKLH/BYT-HTTB
000.00.04.G18-220805-0003
Toxoplasma gondii Real-TM
P1-50FRT
Technical Details
Toxoplasma gondii Real-TM is an in vitro nucleic acid amplification test used to qualitatively determine the presence of Toxoplasma gondii DNA in clinical samples (peripheral blood leukocytes, biopsy samples, cerebrospinal fluid, and amniotic fluid). The PCR analysis results are considered in complex disease diagnosis.
Dates and Status
May 10, 2024