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ONE STEP OVULATION URINE TEST - COFEPRIS Registration 2331R2018 SSA

Access comprehensive regulatory information for ONE STEP OVULATION URINE TEST (ONE STEP OVULATION URINE TEST) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2331R2018 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on October 09, 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 I
2331R2018 SSA
ONE STEP OVULATION URINE TEST
COFEPRIS Analysis ID: 2331R2018 SSA
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Product Use / Uso del Producto
Spanish

PARA LA DETECCIร“N CUALITATIVA DE LA HORMONA LUTEINIZANTE EN ORINA

English

FOR QUALITATIVE DETECTION OF LUTEINIZING HORMONE IN URINE

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)
ENSAYO INMUNOCROMATOGRรFICO PARA LA DETECCIร“N CUALITATIVADE LA HORMONA LUTEINIZANTE (LH)
Trade Name (English)
IMMUNOCHROMATOGRAPHIC ASSAY FOR THE QUALITATIVE DETECTION OF LUTEINIZING HORMONE (LH)
Registration Information
Analysis ID
2331R2018 SSA
Registration Date
October 09, 2018
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.