Mexico COFEPRIS registration 86R2019 SSA

FACTOR VIII DEFICIENT PLASMA

EN: FACTOR VIII DEFICIENT PLASMA
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·REPRESENTACIONES LABIN MEXICO SA DE CV·Registered January 28, 2019
Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACION DEL FACTOR VIII

English

REAGENT FOR THE DETERMINATION OF FACTOR VIII

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACION DEL FACTOR VIII
Trade Name (English)
REAGENT FOR THE DETERMINATION OF FACTOR VIII
Registration information
Analysis ID
86R2019 SSA
Registration Date
January 28, 2019
Manufacturer / Fabricante
Name (English)
REPRESENTATIONS LABIN MEXICO SA DE CV
About this record

Access comprehensive regulatory information for FACTOR VIII DEFICIENT PLASMA (FACTOR VIII DEFICIENT PLASMA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 86R2019 SSA and manufactured by REPRESENTACIONES LABIN MEXICO SA DE CV. The device was registered on January 28, 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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