HELICOBACTER PYLORI IGM ELISA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·INOCHEM SA DE CV·Registered January 28, 2019REACTIVO PARA LA DETERMINACION DE ANTICUERPOS IGM CONTRA HELICOBACTER PYLORI
REAGENT FOR THE DETERMINATION OF IGM ANTIBODIES AGAINST HELICOBACTER PYLORI
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO PARA LA DETERMINACION DE ANTICUERPOS IGM CONTRA HELICOBACTER PYLORI
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF IGM ANTIBODIES AGAINST HELICOBACTER PYLORI
- Analysis ID
- 94R2019 SSA
- Registration Date
- January 28, 2019
- Name (Spanish)
- INOCHEM SA DE CV
- Name (English)
- INOCHEM SA DE CV
Access comprehensive regulatory information for HELICOBACTER PYLORI IGM ELISA (HELICOBACTER PYLORI IGM ELISA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 94R2019 SSA and manufactured by INOCHEM SA DE CV. The device was registered on January 28, 2019.
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.