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INMUNOENSAYO CROMATOGRÁFICO PARA DETERMINACIÓN CUALITATIVO DE ANTÍGENOS DEL SARS-COV- 2, EN MUESTRAS NASOFARINGEAS - COFEPRIS Registration 0155R2024 SSA

Access comprehensive regulatory information for INMUNOENSAYO CROMATOGRÁFICO PARA DETERMINACIÓN CUALITATIVO DE ANTÍGENOS DEL SARS-COV- 2, EN MUESTRAS NASOFARINGEAS (INMUNOENSAYO CROMATOGRÁFICO PARA DETERMINACIÓN CUALITATIVO DE ANTÍGENOS DEL SARS-COV- 2, EN MUESTRAS NASOFARINGEAS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0155R2024 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on January 18, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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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Clase II
0155R2024 SSA
INMUNOENSAYO CROMATOGRÁFICO PARA DETERMINACIÓN CUALITATIVO DE ANTÍGENOS DEL SARS-COV- 2, EN MUESTRAS NASOFARINGEAS
COFEPRIS Analysis ID: 0155R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
STANDARD™ Q COVID-19 AG NASAL TEST
Trade Name (English)
STANDARD™ Q COVID-19 AG NASAL TEST
Registration Information
Analysis ID
0155R2024 SSA
Registration Date
January 18, 2024
Manufacturer / Fabricante
Name (English)
KANA UNDESA, S.A. DE C.V.