Mexico COFEPRIS registration 1014R2024 SSA

PRUEBA TURBIDIMÉTRICA MEJORADA POR LÁTEX PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA

EN: PRUEBA TURBIDIMÉTRICA MEJORADA POR LÁTEX PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·DICIPA, S.A. DE C.V.·Registered April 11, 2024
Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
FERRITIN.
Trade Name (English)
FERRITIN.
Registration information
Analysis ID
1014R2024 SSA
Registration Date
April 11, 2024
Manufacturer / Fabricante
Name (Spanish)
DICIPA, S.A. DE C.V.
Name (English)
DICIPA, S.A. DE C.V.
About this record

Access comprehensive regulatory information for PRUEBA TURBIDIMÉTRICA MEJORADA POR LÁTEX PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA (PRUEBA TURBIDIMÉTRICA MEJORADA POR LÁTEX PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1014R2024 SSA and manufactured by DICIPA, S.A. DE C.V.. The device was registered on April 11, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.

Free DatabasePowered by Pure Global AICOFEPRIS Official DataClase I