TUBOS DE EXTRACCIÓN SANGUÍNEA IMPROVE® CON ANTICOAGULANTE EDTA K2/ EDTA K3 - COFEPRIS Registration 2481R2018 SSA
Access comprehensive regulatory information for TUBOS DE EXTRACCIÓN SANGUÍNEA IMPROVE® CON ANTICOAGULANTE EDTA K2/ EDTA K3 (IMPROVE® BLOOD COLLECTION TUBES WITH ANTICOAGULANT EDTA K2/ EDTA K3) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2481R2018 SSA and manufactured by ATYDE MÉXICO, S.A. DE C.V.. The device was registered on October 26, 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.
TUBOS DE EXTRACCIÓN SANGUÍNEA MODELOS IMPROVACUTER® EDTA K2 TUBE, IMPROVACUTER® EDTA K3 TUBE, IMPROVACUTER® GEL & EDTA K2 TUBE ASI COMO LOS MODELOS IMPROMINI® EDTA K2 TUBE E IMPROMINI® EDTA K3 TUBE SE UTILIZAN PARA LA RECOLECCIÓN, TRANSPORTE Y PROCESADO
BLOOD COLLECTION TUBES MODELS IMPROVACUTER EDTA K2 TUBE, IMPROVACUTER EDTA K3 TUBE, IMPROVACUTER®®® GEL & EDTA K2 TUBE AS WELL AS THE MODELS IMPROMINI EDTA K2 TUBE AND IMPROMINI®® EDTA K3 TUBE ARE USED FOR COLLECTION, TRANSPORT AND PROCESSING