CERTUM CEA RAPID TEST CASSETTE (WHOL BLOOD/SERUM/PLASMA)
INMUNOENSAYO CROMATOGRÁFICO RÁPIDO PARA LA DETECCIÓN DE ACE (ANTÍGENO CARCINOEMBRIONARIO EN LA SANGRE TOTAL, SUERO O PLASMA.
RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE DETECTION OF ACE (CARCINOEMBRYONIC ANTIGEN IN WHOLE BLOOD, SERUM OR PLASMA.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- INMUNOENSAYO CROMATOGRÁFICO RÁPIDO PARA LA DETECCIÓN DE ACE (ANTÍGENO CARCINOEMBRIONARIO)
- Trade Name (English)
- RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE DETECTION OF ACE (CARCINOEMBRYONIC ANTIGEN)
- Analysis ID
- 1180R2019 SSA
- Registration Date
- May 29, 2019
- Name (Spanish)
- KABLA COMERCIAL, S.A. DE C.V.
- Name (English)
- KABLA COMERCIAL, S.A. DE C.V.
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.