STROMATOLYSER™-IM REACTIVO LISANTE - COFEPRIS Registration 2103R2019 SSA
Access comprehensive regulatory information for STROMATOLYSER™-IM REACTIVO LISANTE (STROMATOLYZER-IM™ REACTIVO LISANTE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2103R2019 SSA and manufactured by SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.. The device was registered on November 07, 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.
STROMATOLYSER™-IM ES UN REACTIVO DE LISIS DE LOS ANALIZADORES HEMATOLÓGICOS PARA EL ANÁLISIS DE LEUCOCITOS INMADUROS.
STROMATOLYSER-IM™ IS A LYSIS REAGENT OF HEMATOLOGICAL ANALYZERS FOR THE ANALYSIS OF IMMATURE LEUKOCYTES.