ALINITY C COMPLEMENT C3REAGENT KIT - COFEPRIS Registration 0867R2022 SSA
Access comprehensive regulatory information for ALINITY C COMPLEMENT C3REAGENT KIT (ALINITY C COMPLEMENT C3REAGENT KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0867R2022 SSA and manufactured by ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on September 05, 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.
ELALINITYCCOMPLEMENT C3REAGENT KIT,SE UTILIZAPARALADETERMINACIÓNCUANTITATIVADEC3ENSUEROOPLASMAHUMANOSENELANALIZADORALINITYC.AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARAUSOEXCLUSIVOEN LABORATORIOS CLÍNICOS O DE GABINETE.
ELALINITYCCOMPLEMENT C3REAGENT KIT,SE UTILIZAPARALADETERMINACIÓNCUANTITATIVADEC3ENSUEROOPLASMAHUMANOSENELANALIZADORALINITYC. DIAGNOSTIC AGENTFOR use. FOR USE ONLY IN CLINICAL OR OFFICE LABORATORIES.