Pure Global

BIOELISA HIV 1+2 AG/AB - COFEPRIS Registration 73R2020 SSA

Access comprehensive regulatory information for BIOELISA HIV 1+2 AG/AB (BIOELISA HIV 1+2 AG/AB) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 73R2020 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on February 05, 2020.

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.

Free Database
Powered by Pure Global AI
COFEPRIS Official Data
Clase II
73R2020 SSA
BIOELISA HIV 1+2 AG/AB
COFEPRIS Analysis ID: 73R2020 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

PRUEBA ELISA PARA LA DETECCIÓN DEANTICUERPOS FRENTE A LOS VIRUS DE LAINMUNODEFICIENCIAHUMANA(HIV)DETIPO1(GRUPOM-O)ODETIPO2YANTÍGENOSP24DELHIV EN MUESTRAS HUMANAS DE SUERO OPLASMA.

English

ELISA TEST FOR THE DETECTION OF ANTIBODIES AGAINST HUMAN IMMUNODEFICIENCY VIRUSES (HIV) TYPE 1 (GROUPM-O) ODETYPE2YANTÍGENOSP24DELHIV IN HUMAN SERUM OR PLASMA SAMPLES.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETECCIÓN DEANTICUERPOSANTI-HIV-1YANTI-HIV-2 Y ANTÍGENO P24 DEL HIV
Trade Name (English)
REAGENT FOR THE DETECTION OFANTIBODIESANTI-HIV-1YANTI-HIV-2 AND HIV P24 ANTIGEN
Registration Information
Analysis ID
73R2020 SSA
Registration Date
February 05, 2020
Manufacturer / Fabricante
Name (English)
I.L. DIAGNOSTICS, S.A. DE C.V.