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SMARTPUMP - COFEPRIS Registration 1646E2020 SSA

Access comprehensive regulatory information for SMARTPUMP (SMARTPUMP) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1646E2020 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on December 14, 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
1646E2020 SSA
SMARTPUMP
COFEPRIS Analysis ID: 1646E2020 SSA
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Product Use / Uso del Producto
Spanish

JERINGA: INESTÁINDICADOPARAUTILIZARSEPARAOCLUIRO DISMINUIR TEMPORALMENTE EL FLUJO DESANGREENUNADELASEXTREMIDADESDEUNPACIENTE DURANTE UN PROCEDIMIENTOQUIRÚRGICO DE DICHA EXTREMIDAD.

English

SYRINGE: INDICATED FOR USE TO TEMPORARILY DECREASE BLOOD FLOW IN ONE OF A PATIENT'S LIMBS DURING A SURGICAL PROCEDURE OF THAT LIMB.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
EQUIPO DE TORNIQUETE ROTATORIO
Trade Name (English)
ROTARY TOURNIQUET EQUIPMENT
Registration Information
Analysis ID
1646E2020 SSA
Registration Date
December 14, 2020
Manufacturer / Fabricante
Name (English)
STRYKER MEXICO, S.A. DE C.V.