IGA-C
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DEC.V.·Registered October 12, 2020PRUEBA IN VITRO PARA LA DETERMINACIÓNCUANTITATIVA DE LA INMUNOGLOBULINA A(IGA)ENLÍQUIDOCEFALORRAQUÍDEOHUMANOY DE FORMA PARALELA EN SUERO/PLASMAHUMANO EN LOS SISTEMAS ROCHE
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF IMMUNOGLOBULIN A (IGA) IN CEREBROSPINAL FLUID OR HUMAN AND IN PARALLEL IN HUMAN SERUM / 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 LA INMUNOGLOBULINA A
- Trade Name (English)
- TEST FOR THE DETERMINATION OF IMMUNOGLOBULIN A
- Analysis ID
- 1386R2020 SSA
- Registration Date
- October 12, 2020
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DEC.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DEC.V.
Access comprehensive regulatory information for IGA-C (E-C) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1386R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on October 12, 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.