COULTER DIFF AC • T PAK - COFEPRIS Registration 1882R2019 SSA
Access comprehensive regulatory information for COULTER DIFF AC • T PAK (COULTER DIFF AC • T PAK) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1882R2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on September 19, 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.
PARA USO EN LOS ANALIZADORES HEMATOLÓGICOS COULTER AC • T DIFF Y AC • T DIFF 2 SOLAMENTE. REACTIVO 1: SOLUCIÓN DE ELECTROLITOS EQUILIBRADA COULTER PARA UTILIZAR COMO DILUYENTE TAMPONADO ISOTÓNICO PARA EL RECUENTO Y LA DETERMINACIÓN DEL TAMAÑO DE LAS CÉL
FOR USE IN COULTER AC • T DIFF AND AC • T DIFF 2 HEMATOLOGY ANALYZERS ONLY. REAGENT 1: COULTER BALANCED ELECTROLYTE SOLUTION FOR USE AS ISOTONIC BUFFERED DILUENT FOR CELL COUNTING AND SIZE DETERMINATION