Mexico COFEPRIS registration 0180R2022 SSA

REACTIVO PARA LA MEDICIÓN DE ALBÚMINA EN SUERO O PLASMA

EN: REACTIVO PARA LA MEDICIÓN DE ALBÚMINA EN SUERO O PLASMA
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·AXMILAB, S.A. DE C.V.·Registered March 14, 2022
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)
PKL ALBÚMINA BCG
Trade Name (English)
PKL ALBÚMINA BCG
Registration information
Analysis ID
0180R2022 SSA
Registration Date
March 14, 2022
Manufacturer / Fabricante
Name (Spanish)
AXMILAB, S.A. DE C.V.
Name (English)
AXMILAB, S.A. DE C.V.
About this record

Access comprehensive regulatory information for REACTIVO PARA LA MEDICIÓN DE ALBÚMINA EN SUERO O PLASMA (REACTIVO PARA LA MEDICIÓN DE ALBÚMINA EN SUERO O PLASMA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0180R2022 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on March 14, 2022.

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