DIINSELMULTIPLEDRUGSTESTCUP - COFEPRIS Registration 375R2022 SSA
Access comprehensive regulatory information for DIINSELMULTIPLEDRUGSTESTCUP (DIINSELMULTIPLEDRUGSTESTCUP) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 375R2022 SSA and manufactured by DIINSEL, S.A. DE C.V.. The device was registered on May 13, 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.
DIINSELMULTIPLEDRUGSTESTCUPESUNINMUNOENSAYOVISUAL RÁPIDO PARA LA DETECCIÓN CUALITATIVA DEDROGAS DE ABUSO EN MUESTRAS DE FLUIDO ORALHUMANO. AGENTEDEDIAGNÓSTICOINVITRO.PARAUSOEXCLUSIVO DE LABORATORIO CLÍNICO O DE GABINETE
DIINSELMULTIPLEDRUGSTESTCUPESA RAPID VISUAL IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF DRUGS OF ABUSE IN HUMAN ORAL FLUID SAMPLES. DIAGNOSTICAGENTINVITRO. FOR CLINICAL LABORATORY OR CABINET USE ONLY