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CYSC2 - COFEPRIS Registration 1615R2020 SSA

Access comprehensive regulatory information for CYSC2 (CYSC2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1615R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on December 04, 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
1615R2020 SSA
CYSC2
COFEPRIS Analysis ID: 1615R2020 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO DE DIAGNÓSTICO IN VITRO PARACISTATINA C

English

IN VITRO PARACIST DIAGNOSTIC REAGENT C

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVODEDIAGNÓSTICOINVITROPARA CISTATINA C
Trade Name (English)
REACTIVODEDIAGNÓSTICOINVITROPARA CISTATINA C
Registration Information
Analysis ID
1615R2020 SSA
Registration Date
December 04, 2020
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DEC.V.