REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA
Mexico·Clase I·III. Agentes de diagnóstico·LAB-CENTER DE
MÉXICO S.A. DE C.V.·Registered October 27, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- ALP-LQ
- Trade Name (English)
- ALP-LQ
- Analysis ID
- 1208R2022 SSA
- Registration Date
- October 27, 2022
- Name (Spanish)
- LAB-CENTER DE MÉXICO S.A. DE C.V.
- Name (English)
- LAB-CENTER DE MÉXICO S.A. DE C.V.
Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA (REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1208R2022 SSA and manufactured by LAB-CENTER DE MÉXICO S.A. DE C.V.. The device was registered on October 27, 2022.
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.