ALBP
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered February 24, 2020PARALADETERMINACIÓNCUANTITATIVADELAALBÚMINAENSUEROYPLASMAHUMANOSENLOS SISTEMAS ROCHE.
FOR THE QUANTITATIVE DETERMINATION OF ALBUMININ HUMAN 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 DETERMINACIÓNDE LA ALBÚMINA
- Trade Name (English)
- TEST FOR THE DETERMINATION OF ALBUMIN
- Analysis ID
- 212R2020 SSA
- Registration Date
- February 24, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
Access comprehensive regulatory information for ALBP (ALBP) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 212R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on February 24, 2020.
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.