ONE STEP OVULATION URINE TEST
Mexico·Clase I·III. DIAGNOSTIC AGENTS·KABLA COMERCIAL, S.A. DE C.V.·Registered October 09, 2018PARA LA DETECCIÓN CUALITATIVA DE LA HORMONA LUTEINIZANTE EN ORINA
FOR QUALITATIVE DETECTION OF LUTEINIZING HORMONE IN URINE
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO INMUNOCROMATOGRÁFICO PARA LA DETECCIÓN CUALITATIVADE LA HORMONA LUTEINIZANTE (LH)
- Trade Name (English)
- IMMUNOCHROMATOGRAPHIC ASSAY FOR THE QUALITATIVE DETECTION OF LUTEINIZING HORMONE (LH)
- Analysis ID
- 2331R2018 SSA
- Registration Date
- October 09, 2018
- Name (Spanish)
- KABLA COMERCIAL, S.A. DE C.V.
- Name (English)
- KABLA COMERCIAL, S.A. DE C.V.
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.