REAGENTKITFORPREALBUMINKIT(PA) MINDRAY
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.·Registered February 12, 2021PRUEBAS PARA DETERMINACIÓNCUANTITATIVADELACONCENTRACIÓNDEPAMEN SUERO EN SISTEMAS FOTOMÉTRICOS
TESTS FOR QUANTITATIVE DETERMINATION OF SERUM CONCENTRATION IN PHOTOMETRIC SYSTEMS
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO PARA LA DETERMINACIÓN DEPREALBÚMINA MEDIANTE MÉTODO DETURBIDIMÉTRICO
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF PREALBUMIN BY METHOD DETURBIDIMÉTRICO
- Analysis ID
- 2039R2021 SSA
- Registration Date
- February 12, 2021
- Name (Spanish)
- MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.
- Name (English)
- MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.
Access comprehensive regulatory information for REAGENTKITFORPREALBUMINKIT(PA) MINDRAY (REAGENTKITFORPREALBUMINKIT(PA) MINDRAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2039R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on February 12, 2021.
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.