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INYECTOR DE DIÓXIDO DECARBONO, ANGIODROID - COFEPRIS Registration 32E2020 SSA

Access comprehensive regulatory information for INYECTOR DE DIÓXIDO DECARBONO, ANGIODROID (CARBON DIOXIDE INJECTOR, ANGIODROID) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 32E2020 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on January 10, 2020.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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 II
32E2020 SSA
INYECTOR DE DIÓXIDO DECARBONO, ANGIODROID
COFEPRIS Analysis ID: 32E2020 SSA
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Product Use / Uso del Producto
Spanish

DISPOSITIVO QUE PERMITE LA INYECCIÓN DEDIÓXIDO DE CARBONO, PARA OBTENERIMÁGENESRADIOLÓGICASPARADIAGNÓSTICO.PARAREALIZARUNAANGIOGRAFÍAPERIFÉRICADIAGNÓSTICA E INTERVENCIONISTA.

English

DEVICE THAT ALLOWS THE INJECTION OFCARBON DIOXIDE, TO OBTAIN RADIOLOGICAL IMAGES FOR DIAGNOSIS. TO PERFORM A DIAGNOSTIC AND INTERVENTIONAL PERIPHERAL ANGIOGRAPHY.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
INYECTOR PARA USO ANGIOGRÁFICO
Trade Name (English)
INJECTOR FOR ANGIOGRAPHIC USE
Registration Information
Analysis ID
32E2020 SSA
Registration Date
January 10, 2020
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL S.A. DE C.V.