LIQUICHEK™ URINE TOXICOLOGY CONTROL - COFEPRIS Registration 1173R2018 SSA
Access comprehensive regulatory information for LIQUICHEK™ URINE TOXICOLOGY CONTROL (LIQUICHEK™ URINE TOXICOLOGY CONTROL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1173R2018 SSA and manufactured by BIO-RAD, S.A.. The device was registered on May 23, 2018.
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.
LIQUICHEK™ URINE TOXICOLOGY CONTROL TIENE UN USO INTENCIONADO COMO ORINA PARA EL CONTROL DE LA CALIDAD Y CON EL FIN DE SUPERVISAR LOS PROCEDIMIENTOS DE CONFIRMACION EN TOXICOLOGIA DE ORINA DEL LABORATORIO. AGENTE DE DIAGNÓSTICO IN VITRO. PARA USO EXCLUSIV
LIQUICHEK™ URINE TOXICOLOGY CONTROL HAS AN INTENDED USE AS URINE FOR QUALITY CONTROL AND IN ORDER TO SUPERVISE THE LABORATORY'S URINE TOXICOLOGY CONFIRMATION PROCEDURES. IN VITRO DIAGNOSTIC AGENT. FOR EXCLUSIVE USE