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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.

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COFEPRIS Official Data
Clase I
1180R2019 SSA
CERTUM CEA RAPID TEST CASSETTE (WHOL BLOOD/SERUM/PLASMA)
COFEPRIS Analysis ID: 1180R2019 SSA
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Product Use / Uso del Producto
Spanish

INMUNOENSAYO CROMATOGRรFICO RรPIDO PARA LA DETECCIร“N DE ACE (ANTรGENO CARCINOEMBRIONARIO EN LA SANGRE TOTAL, SUERO O PLASMA.

English

RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE DETECTION OF ACE (CARCINOEMBRYONIC ANTIGEN IN WHOLE BLOOD, SERUM OR PLASMA.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
INMUNOENSAYO CROMATOGRรFICO RรPIDO PARA LA DETECCIร“N DE ACE (ANTรGENO CARCINOEMBRIONARIO)
Trade Name (English)
RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE DETECTION OF ACE (CARCINOEMBRYONIC ANTIGEN)
Registration Information
Analysis ID
1180R2019 SSA
Registration Date
May 29, 2019
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.