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ELECSYS ZIKA IGG - COFEPRIS Registration 1399R2020 SSA

Access comprehensive regulatory information for ELECSYS ZIKA IGG (ELECSYS ZIKA IGG) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1399R2020 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.

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COFEPRIS Official Data
Clase I
1399R2020 SSA
ELECSYS ZIKA IGG
COFEPRIS Analysis ID: 1399R2020 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA INMUNOLร“GICA IN VITRO PARA LADETERMINACIร“N CUALITATIVA DEANTICUERPOSIGGFRENTEALVIRUSDELZIKAEN SUERO Y PLASMA HUMANOS.

English

IN VITRO IMMUNOLOGICAL TEST FOR THE QUALITATIVE DETERMINATION OF SIGGANTIG ANTIBODY AGAINST ZIKA VIRUS IN HUMAN SERUM AND PLASMA.

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)
PRUEBA PARA LA DETERMINACIร“NDEANTICUERPOSIGGDELVIRUSDELZIKA
Trade Name (English)
TEST FOR THE DETERMINATION OF SIGGDELZIKA VIRUS ANTIBODY
Registration Information
Analysis ID
1399R2020 SSA
Registration Date
October 12, 2020
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DEC.V.