CERTUM CEA RAPID TEST CASSETTE (WHOL BLOOD/SERUM/PLASMA) - COFEPRIS Registration 1180R2019 SSA
Access comprehensive regulatory information for CERTUM CEA RAPID TEST CASSETTE (WHOL BLOOD/SERUM/PLASMA) (CERTUM CEA RAPID TEST CASSETTE (WHOL BLOOD/SERUM/PLASMA)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1180R2019 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on May 29, 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.
INMUNOENSAYO CROMATOGRรFICO RรPIDO PARA LA DETECCIรN DE ACE (ANTรGENO CARCINOEMBRIONARIO EN LA SANGRE TOTAL, SUERO O PLASMA.
RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE DETECTION OF ACE (CARCINOEMBRYONIC ANTIGEN IN WHOLE BLOOD, SERUM OR PLASMA.

