UF-REAGENTS
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.·Registered May 23, 2018LOS UF-REAGENTS SE UTILIZAN PARA PARA EL DIAGNÓSTICO IN VITRO, A TRAVÉS LA DETERMINACIÓN DE LOS PARÁMETROS CLÍNICOS QUE SE REALIZA EN CONJUNTO CON LOS ANALIZADORES AUTOMATIZADOS DE PARTÍCULAS DE ORINA Y OTROS LÍQUIDOS CORPORALES SYSMEX, LOS CUALES SE DESC
UF-REAGENTS ARE USED FOR IN VITRO DIAGNOSTICS, THROUGH THE DETERMINATION OF CLINICAL PARAMETERS THAT IS PERFORMED IN CONJUNCTION WITH SYSMEX AUTOMATED ANALYZERS OF URINE PARTICLES AND OTHER BODY FLUIDS, WHICH ARE DESC
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVOS PARA ANALIZADORES AUTOMATIZADOS DE PARTÍCULAS DE ORINA Y OTROS LÍQUIDOS CORPORALES
- Trade Name (English)
- REAGENTS FOR AUTOMATED ANALYZERS OF URINE PARTICLES AND OTHER BODY FLUIDS
- Analysis ID
- 1179R2018 SSA
- Registration Date
- May 23, 2018
- Name (Spanish)
- SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.
- Name (English)
- SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.
Access comprehensive regulatory information for UF-REAGENTS (UF-REAGENTS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1179R2018 SSA and manufactured by SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.. The device was registered on May 23, 2018.
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.