REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE 25-OH VIT-D EN SUERO O PLASMA HUMANO.
Mexico·Clase I·III. Agentes de
diagnóstico·ATYDE MÉXICO S.A. DE C.V.·Registered January 31, 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)
- 25-OH VITAMIN D (25-OH VIT-D) TEST KIT (IMMUNOFLUORESCENCE) GENRUI
- Trade Name (English)
- 25-OH VITAMIN D (25-OH VIT-D) TEST KIT (IMMUNOFLUORESCENCE) GENRUI
- Analysis ID
- 0331R2024 SSA
- Registration Date
- January 31, 2024
- Name (Spanish)
- ATYDE MÉXICO S.A. DE C.V.
- Name (English)
- ATYDE MÉXICO S.A. DE C.V.
Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE 25-OH VIT-D EN SUERO O PLASMA HUMANO. (REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE 25-OH VIT-D EN SUERO O PLASMA HUMANO.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0331R2024 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on January 31, 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.