ACP2
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered March 17, 2020PRUEBA IN VITRO PARA LA DETERMINACIÓNCUANTITATIVA DE LA FOSFATASA ÁCIDA ENSUERO HUMANO EN LOS SISTEMAS ROCHE.
IN VITRO TEST FOR QUANTITATIVE DETERMINATION OF ACID PHOSPHATASE IN HUMAN SERUM 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 FOSFATASA ÁCIDA.
- Trade Name (English)
- TEST FOR THE DETERMINATION OF ACID PHOSPHATASE.
- Analysis ID
- 325R2020 SSA
- Registration Date
- March 17, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
Access comprehensive regulatory information for ACP2 (ACP2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 325R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on March 17, 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.