IMMUNOLOGY KIT FERRITIN MINDRAY
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MINDRAY MEDICAL MÉXICO, S. DE R.L. DE C.V.·Registered June 05, 2018KIT DE REACTIVOS PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA (FERR) A TRAVÉS DE UN INMUNOENSAYO DE QUIMIOLUMINISCENCIA (CLIA) EN PLASMA O SUERO HUMANOS.
KIT OF REAGENTS FOR THE QUANTITATIVE DETERMINATION OF FERRITIN (FERR) THROUGH A CHEMILUMINESCENCE IMMUNOASSAY (CLIA) IN HUMAN PLASMA OR SERUM.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- KIT PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA
- Trade Name (English)
- KIT FOR THE QUANTITATIVE DETERMINATION OF FERRITIN
- Analysis ID
- 1371R2018 SSA
- Registration Date
- June 05, 2018
- Name (Spanish)
- MINDRAY MEDICAL MÉXICO, S. DE R.L. DE C.V.
- Name (English)
- MINDRAY MEDICAL MEXICO, S. DE R.L. DE C.V.
Access comprehensive regulatory information for IMMUNOLOGY KIT FERRITIN MINDRAY (IMMUNOLOGY KIT FERRITIN 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 1371R2018 SSA and manufactured by MINDRAY MEDICAL MÉXICO, S. DE R.L. DE C.V.. The device was registered on June 05, 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.