ANTI-MUMPS VIRUS ELISA (IGM) - COFEPRIS Registration 0853R2022 SSA
Access comprehensive regulatory information for ANTI-MUMPS VIRUS ELISA (IGM) (ANTI-MUMPS VIRUS ELISA (IGM)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0853R2022 SSA and manufactured by INOCHEM SA DE CV. The device was registered on August 01, 2022.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
ELPRESENTEEQUIPODEENSAYOELISA SIRVEPARA LADETERMINACIÓN IN VITRO SEMICUANTITATIVA DEANTICUERPOS HUMANOS DE LA CLASE DEINMUNOGLOBULINAIGMCONTRAELVIRUSDELASPAPERASEN SUERO O PLASMA PARA EL DIAGNÓSTICO DE LASPAPERAS. AGENTE DE DIAGNÓSTICO
THE PRESENT ELISA ASSAY IS USED FOR THE SEMI-QUANTITATIVE IN VITRO DETERMINATION OF HUMAN ANTIBODIES OF THE IMMUNOGLOBULIN CLASS IGM AGAINST MUMPS VIRUS IN SERUM OR PLASMA FOR THE DIAGNOSIS OF MUMPS. DIAGNOSTIC AGENT