KIT PARA LA HORMONAADENOCORTICOTRÓPICA (ACTH)MINDRAY - COFEPRIS Registration 2052R2021 SSA
Access comprehensive regulatory information for KIT PARA LA HORMONAADENOCORTICOTRÓPICA (ACTH)MINDRAY (HORMONE ADENOCORTICOTROPIC HORMONE KIT (ACTH)MINDRAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2052R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on March 12, 2021.
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.
EL ENSAYO DE ACTH SERIE CL ES UNINMUNOENSAYO DE QUIMIOLUMINISCENCIA(CLI)PARALADETERMINACIÓNCUANTITATIVADELA HORMONA ADRENOCORTICOTRÓPICA(ACTH) EN EL PLASMA EDTA HUMANO.AGENTE DE DIAGNÓSTICO IN VITRO PARA
THE ACTH CL SERIES ASSAY IS A CHEMILUMINESCENCE IMMUNOASSAY (CLI) FOR THE QUANTITATIVE DETERMINATION OF ADRENOCORTICOTROPIC HORMONE (ACTH) IN HUMAN EDTA PLASMA. IN VITRO DIAGNOSTIC AGENT FOR