MDMULTICARD ABO-D CONFIRM FOR DONORS - COFEPRIS Registration 1851R2019 SSA
Access comprehensive regulatory information for MDMULTICARD ABO-D CONFIRM FOR DONORS (MDMULTICARD ABO-D CONFIRM FOR DONORS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1851R2019 SSA and manufactured by GRIFOLS MÉXICO, S.A. DE C.V.. The device was registered on September 13, 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.
TIPAJE SIMULTÁNEO DE LOS GRUPOS SANGUÍNEOS ABO Y RH UTILIZANDO EL PRINCIPIO DE INMUNOCROMATOGRAFÍA DE FLUJO LATERAL. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO DE LABORATORIOS DE CLÍNICOS O DE GABINETE.
SIMULTANEOUS TYPING OF ABO AND RH BLOOD GROUPS USING THE PRINCIPLE OF LATERAL FLOW IMMUNOCHROMATOGRAPHY. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR EXCLUSIVE USE OF CLINICAL OR CABINET LABORATORIES.