Pure Global

FTD FEVER AND RASH - COFEPRIS Registration 542R2019 SSA

Access comprehensive regulatory information for FTD FEVER AND RASH (FTD FEVER AND RASH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 542R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on March 14, 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.

Free Database
Powered by Pure Global AI
COFEPRIS Official Data
Clase I
542R2019 SSA
FTD FEVER AND RASH
COFEPRIS Analysis ID: 542R2019 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

ENSAYO PARA DETERMINAR ACIDOS NUCLEICOS

English

NUCLEIC ACID ASSAY

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)
ENSAYO PARA DETERMINAR ACIDOS NUCLEICOS
Trade Name (English)
NUCLEIC ACID ASSAY
Registration Information
Analysis ID
542R2019 SSA
Registration Date
March 14, 2019
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR