ALP2
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DE C.V.·Registered October 10, 2019PRUEBA IN VITRO PARA LA DETERMINACIÓN CUANTITATIVA DE LA FOSFATASA ALCALINA EN SUERO Y PLASMA HUMANOS EN LOS SISTEMAS ROCHE.
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF ALKALINE PHOSPHATASE IN HUMAN SERUM AND PLASMA IN ROCHE SYSTEMS.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA LA DETERMINACIÓN DE LA FOSFATASA ALCALINA
- Trade Name (English)
- TEST FOR THE DETERMINATION OF ALKALINE PHOSPHATASE
- Analysis ID
- 1969R2019 SSA
- Registration Date
- October 10, 2019
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for ALP2 (ALP2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1969R2019 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on October 10, 2019.
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.