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STREP-A RESPI-STRIP CORIS BIOCONCEPT - COFEPRIS Registration 2338R2018 SSA

Access comprehensive regulatory information for STREP-A RESPI-STRIP CORIS BIOCONCEPT (STREP-A RESPI-STRIP CORIS BIOCONCEPT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2338R2018 SSA and manufactured by PHARMACUR, S.A. DE C.V.. The device was registered on October 11, 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.

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COFEPRIS Official Data
Clase I
2338R2018 SSA
STREP-A RESPI-STRIP CORIS BIOCONCEPT
COFEPRIS Analysis ID: 2338R2018 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA RรPIDA DE DIAGNร“STICO IN VITRO PARA DETECCIร“N DE INFECCIร“N HUMANA POR ESTREPTOCOCO GRUPO A EN MUESTRAS DE HISOPO FARรNGEO

English

RAPID IN VITRO DIAGNOSTIC TEST FOR DETECTION OF HUMAN GROUP A STREPTOCOCCAL INFECTION IN PHARYNGEAL SWAB SAMPLES

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)
PRUEBA PARA DETECCIร“N DE ESTREPTOCOCOS
Trade Name (English)
STREPTOCOCCAL TEST
Registration Information
Analysis ID
2338R2018 SSA
Registration Date
October 11, 2018
Manufacturer / Fabricante
Name (English)
PHARMACUR, S.A. DE C.V.