UIBC
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered September 15, 2020PRUEBA IN VITRO PARA DETERMINACIÓNCUANTITATIVADELACAPACIDADLATENTEDEFIJACIÓN DE HIERRO EN SUERO Y PLASMAHUMANOS EN LOS SISTEMAS ROCHE
IN VITRO TEST FOR QUANTITATIVE DETERMINATION OF LATENT IRON FIXATION CAPACITY IN HUMAN SERUM AND PLASMA IN ROCHE SYSTEMS
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA LA DETERMINACIÓNDE FIJACIÓN DE HIERRO
- Trade Name (English)
- TEST FOR THE DETERMINATION OF IRON FIXATION
- Analysis ID
- 1258R2020 SSA
- Registration Date
- September 15, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
Access comprehensive regulatory information for UIBC (UIBC) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1258R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on September 15, 2020.
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.