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ANTICUERPOS ANTI-NUCLEOSOMA - COFEPRIS Registration 1395R2019 SSA

Access comprehensive regulatory information for ANTICUERPOS ANTI-NUCLEOSOMA (ANTI-NUCLEOSOME ANTIBODIES) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1395R2019 SSA and manufactured by BIO SIMEX, S.A. DE C.V.. The device was registered on July 18, 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 II
1395R2019 SSA
ANTICUERPOS ANTI-NUCLEOSOMA
COFEPRIS Analysis ID: 1395R2019 SSA
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Product Use / Uso del Producto
Spanish

PARA LA DETERMINACIร“N CUALITATIVA Y CUANTITATIVA DE ANTICUERPOS ANTI-NUCLEOSOMA EN SUERO O PLASMA HUMANOS.

English

FOR THE QUALITATIVE AND QUANTITATIVE DETERMINATION OF ANTI-NUCLEOSOME ANTIBODIES IN HUMAN SERUM OR PLASMA.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVOS PARA LA DETERMINACIร“N DE ANTICUERPOS ANTI-NUCLEOSOMA
Trade Name (English)
REAGENTS FOR THE DETERMINATION OF ANTI-NUCLEOSOME ANTIBODIES
Registration Information
Analysis ID
1395R2019 SSA
Registration Date
July 18, 2019
Manufacturer / Fabricante
Name (English)
BIO SIMEX, S.A. DE C.V.