ADPTEST
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered March 20, 2020PRUEBA IN VITRO PARA LA DETERMINACIÓNCUANTITATIVA DE LA FUNCIÓN PLAQUETARIATRAS LA ESTIMULACIÓN DE LOS RECEPTORESPLAQUETARIOSDELDIFOSFATODEADENOSINA(ADP). EL PRESENTE REACTIVO ESTÁCONCEBIDO PARA EL ANÁLISIS DE LAAGREGACIÓN PLAQUETARIA ENMUESTRASDESANGRE TOTAL PROCESADAS CON LOSANALIZADORES ROCHE.
IN VITRO TEST FOR QUANTITATIVE DETERMINATION OF PLATELET FUNCTION STIMULATION OF PLATELET RECEPTORS DIPHOSPHATEDEADENOSINE (ADP). THIS REAGENT IS DESIGNED FOR THE ANALYSIS OF PLATELET AGGREGATION IN WHOLE BLOOD SAMPLES PROCESSED WITH ROCHE ANALYSERS.
- 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 FUNCIÓN PLAQUETARIA.
- Trade Name (English)
- TEST FOR THE DETERMINATION OF PLATELET FUNCTION.
- Analysis ID
- 354R2020 SSA
- Registration Date
- March 20, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
Access comprehensive regulatory information for ADPTEST (ADPTEST) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 354R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on March 20, 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.