AESKULISA® CROHN’S-CHECK - COFEPRIS Registration 1335R2019 SSA
Access comprehensive regulatory information for AESKULISA® CROHN’S-CHECK (AESKULISA® CROHN'S-CHECK) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1335R2019 SSA and manufactured by GRIFOLS MÉXICO, S.A. DE C.V.. The device was registered on July 16, 2019.
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.
ES UN ENZIMOINMUNOENSAYO EN FASE SÓLIDA (ELISA) QUE EMPLEA MANANO ELEVADAMENTE PURIFICADO PARA LA DETECCIÓN COMBINADA CUANTITATIVA Y CUALITATIVA DE ANTICUERPOS ANTI-SACCHAROMYCES CEREVISIAE IGA E IGG (ASCA) EN SUERO HUMANO.
IT IS A SOLID-PHASE ENZYME IMMUNOASSAY (ELISA) THAT USES HIGHLY PURIFIED MANNAN FOR THE COMBINED QUANTITATIVE AND QUALITATIVE DETECTION OF ANTI-SACCHAROMYCES CEREVISIAE IGA AND IGG (ASCA) ANTIBODIES IN HUMAN SERUM.