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PROGESTERONE (CLIA) WIENER LAB - COFEPRIS Registration 618R2019 SSA

Access comprehensive regulatory information for PROGESTERONE (CLIA) WIENER LAB (PROGESTERONE (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 618R2019 SSA and manufactured by REPRESENTACIONES LABIN MEXICO SA DE CV. The device was registered on March 27, 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 I
618R2019 SSA
PROGESTERONE (CLIA) WIENER LAB
COFEPRIS Analysis ID: 618R2019 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACION DE PROGESTERONA

English

REAGENT FOR THE DETERMINATION OF PROGESTERONE

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACION DE PROGESTERONA
Trade Name (English)
REAGENT FOR THE DETERMINATION OF PROGESTERONE
Registration Information
Analysis ID
618R2019 SSA
Registration Date
March 27, 2019
Manufacturer / Fabricante
Name (English)
REPRESENTATIONS LABIN MEXICO SA DE CV