EUROPLUS GRANULOCYTE MOSAIC 25
Mexico·Clase I·III. DIAGNOSTIC AGENTS·INOCHEM SA DE CV·Registered February 22, 2018PARA DETERMINACIÓN IN VITRO DE ANTICUERPOS HUMANOS DE LA CLASE INMUNOGLOBULINA IGG CONTRA CITOPLASMA ANCA
FOR IN VITRO DETERMINATION OF HUMAN ANTIBODIES OF THE IMMUNOGLOBULIN IGG CLASS AGAINST ANCA CYTOPLASM
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA DETERMINACIÓN DE AUTOANTICUERPOS CONTRA IGG
- Trade Name (English)
- ASSAY FOR DETERMINATION OF AUTOANTIBODIES AGAINST IGG
- Analysis ID
- 507R2018 SSA
- Registration Date
- February 22, 2018
- Name (Spanish)
- INOCHEM SA DE CV
- Name (English)
- INOCHEM SA DE CV
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.