PRUEBA DE OVULACIÓN
Mexico·Clase I·III. Agentes de
diagnóstico·MANDALA MÉXICO LEGAL
AFFAIRS, S.A. DE C.V.·Registered March 14, 2024- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- HEALGEN OVULATION RAPID TEST CASSETTE, PRUEBA DE OVULACIÓN
- Trade Name (English)
- HEALGEN OVULATION RAPID TEST CASSETTE, PRUEBA DE OVULACIÓN
- Analysis ID
- 0729R2024 SSA
- Registration Date
- March 14, 2024
- Name (Spanish)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
- Name (English)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA DE OVULACIÓN (PRUEBA DE OVULACIÓN) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0729R2024 SSA and manufactured by MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.. The device was registered on March 14, 2024.
This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.