PRUEBA RÁPIDA EN CARTUCHO PARA LA DETECCIÓN SEMICUANTITATIVA DE LA 25 HIDROXIVITAMINA D (25(OH)D)
Mexico·Clase I·III. Agentes de
diagnóstico·AMUNET, S.A. DE C.V.·Registered January 25, 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)
- VITAMINET D
- Trade Name (English)
- VITAMINET D
- Analysis ID
- 0252R2024 SSA
- Registration Date
- January 25, 2024
- Name (Spanish)
- AMUNET, S.A. DE C.V.
- Name (English)
- AMUNET, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA RÁPIDA EN CARTUCHO PARA LA DETECCIÓN SEMICUANTITATIVA DE LA 25 HIDROXIVITAMINA D (25(OH)D) (PRUEBA RÁPIDA EN CARTUCHO PARA LA DETECCIÓN SEMICUANTITATIVA DE LA 25 HIDROXIVITAMINA D (25(OH)D)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0252R2024 SSA and manufactured by AMUNET, S.A. DE C.V.. The device was registered on January 25, 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.