Mexico COFEPRIS registration 712R2019 SSA

PROLACTIN (CLIA) WIENER LAB

EN: PROLACTIN (CLIA) WIENER LAB
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·REPRESENTACIONES LABIN MEXICO SA DE CV·Registered April 08, 2019
Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACION DE PROLACTINA (PRL)

English

REAGENT FOR THE DETERMINATION OF PROLACTIN (PRL)

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 DE PROLACTINA (PRL)
Trade Name (English)
REAGENT FOR THE DETERMINATION OF PROLACTIN (PRL)
Registration information
Analysis ID
712R2019 SSA
Registration Date
April 08, 2019
Manufacturer / Fabricante
Name (English)
REPRESENTATIONS LABIN MEXICO SA DE CV
About this record

Access comprehensive regulatory information for PROLACTIN (CLIA) WIENER LAB (PROLACTIN (CLIA) WIENER LAB) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 712R2019 SSA and manufactured by REPRESENTACIONES LABIN MEXICO SA DE CV. The device was registered on April 08, 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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