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BSA 22% Y BSA 30% - COFEPRIS Registration 1469R2018 SSA

Access comprehensive regulatory information for BSA 22% Y BSA 30% (BSA 22% Y BSA 30%) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1469R2018 SSA and manufactured by INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.. The device was registered on June 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 II
1469R2018 SSA
BSA 22% Y BSA 30%
COFEPRIS Analysis ID: 1469R2018 SSA
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Product Use / Uso del Producto
Spanish

LA ALBÚMINA DE SUERO BOVINO BSA 22% Y BSA 30% SE USAN PARA AUMENTAR LA INTENSIDAD DE LOS REACTIVOS SEROLÓGICOS. AGENTE DE DIAGNÓSTICO IN VITRO, PARA USO EXCLUSIVO DE LABORATORIO CLÍNICO O DE GABINETE.

English

BSA BOVINE SERUM ALBUMIN 22% AND BSA 30% ARE USED TO INCREASE THE INTENSITY OF SEROLOGICAL REAGENTS. IN VITRO DIAGNOSTIC AGENT, FOR CLINICAL LABORATORY OR CABINET USE ONLY.

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)
ALBÚMINA SÉRICA BOVINA
Trade Name (English)
BOVINE SERUM ALBUMIN
Registration Information
Analysis ID
1469R2018 SSA
Registration Date
June 11, 2018
Manufacturer / Fabricante
Name (English)
INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.