Pure Global

SPEEDTRAP SISTEMA DE PREPARACIÓN DEL INJERTO - COFEPRIS Registration 578C2019 SSA

Access comprehensive regulatory information for SPEEDTRAP SISTEMA DE PREPARACIÓN DEL INJERTO (SPEEDTRAP GRAFT PREPARATION SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 578C2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on March 20, 2019.

This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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 III
578C2019 SSA
SPEEDTRAP SISTEMA DE PREPARACIÓN DEL INJERTO
COFEPRIS Analysis ID: 578C2019 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

SISTEMA DE PREPARACIÓN DEL INJERTO

English

GRAFT PREPARATION SYSTEM

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
SISTEMA DE PREPARACIÓN DEL INJERTO
Trade Name (English)
GRAFT PREPARATION SYSTEM
Registration Information
Analysis ID
578C2019 SSA
Registration Date
March 20, 2019
Manufacturer / Fabricante
Name (English)
JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.