REAGENT KIT FOR IRON (FE)MINDRAY.
PRUEBASINVITROPARALADETERMINACIÓNCUANTITATIVA DE HIERRO EN SUERO YPLASMA HEPARINIZADO HUMANOS ENSISTEMAS FOTOMÉTRICOS. AGENTE DEDIAGNÓSTICOPARAUSOINVITRO. PARAUSOEXCLUSIVO EN LABORATORIOS CLÍNICOS O
TESTSINVITROPARADELA QUANTITATIVE DETERMINATION OF IRON IN HUMAN SERUM AND HEPARINIZED PLASMA IN PHOTOMETRIC SYSTEMS. DIAGNOSTIC AGENTFORUSEINVITRO. FOR EXCLUSIVE USE IN CLINICAL LABORATORIES OR
- 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 DEHIERRO.
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OFIRON.
- Analysis ID
- 2120R2021 SSA
- Registration Date
- December 14, 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 REAGENT KIT FOR IRON (FE)MINDRAY. (REAGENT KIT FOR IRON (FE)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 2120R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on December 14, 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.