Pure Global

EUROPLUS GRANULOCYTE MOSAIC 25 - COFEPRIS Registration 507R2018 SSA

Access comprehensive regulatory information for EUROPLUS GRANULOCYTE MOSAIC 25 (EUROPLUS GRANULOCYTE MOSAIC 25) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 507R2018 SSA and manufactured by INOCHEM SA DE CV. The device was registered on February 22, 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.

Free Database
Powered by Pure Global AI
COFEPRIS Official Data
Clase I
507R2018 SSA
EUROPLUS GRANULOCYTE MOSAIC 25
COFEPRIS Analysis ID: 507R2018 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

PARA DETERMINACIร“N IN VITRO DE ANTICUERPOS HUMANOS DE LA CLASE INMUNOGLOBULINA IGG CONTRA CITOPLASMA ANCA

English

FOR IN VITRO DETERMINATION OF HUMAN ANTIBODIES OF THE IMMUNOGLOBULIN IGG CLASS AGAINST ANCA CYTOPLASM

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
ENSAYO PARA DETERMINACIร“N DE AUTOANTICUERPOS CONTRA IGG
Trade Name (English)
ASSAY FOR DETERMINATION OF AUTOANTIBODIES AGAINST IGG
Registration Information
Analysis ID
507R2018 SSA
Registration Date
February 22, 2018
Manufacturer / Fabricante
Name (Spanish)
INOCHEM SA DE CV
Name (English)
INOCHEM SA DE CV