ASTP
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DE C.V.·Registered July 17, 2019PRUEBA IN VITRO PARA LA DETERMINACIÓN CUANTITATIVA DE LA ASPARTATO AMINOTRANSFERASA (AST) CON ACTIVACIÓN POR FOSFATO DE PIRIDOXAL EN SUERO Y PLASMA HUMANOS EN LOS SISTEMAS ROCHE. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORI
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF ASPARTATE AMINOTRANSFERASE (AST) WITH PYRIDOXAL PHOSPHATE ACTIVATION IN HUMAN SERUM AND PLASMA IN ROCHE SYSTEMS. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR EXCLUSIVE USE IN LABORATORI
- 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 ASPARTATO AMINOTRANSFERASA (AST).
- Trade Name (English)
- TEST FOR THE DETERMINATION OF ASPARTATE AMINOTRANSFERASE (AST).
- Analysis ID
- 1362R2019 SSA
- Registration Date
- July 17, 2019
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for ASTP (ASTP) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1362R2019 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on July 17, 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.