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EXPRESSEW® III AUTOCAPTURE+ - COFEPRIS Registration 954E2019 SSA

Access comprehensive regulatory information for EXPRESSEW® III AUTOCAPTURE+ (EXPRESSEW® III AUTOCAPTURE+) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 954E2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on May 09, 2019.

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 I
954E2019 SSA
EXPRESSEW® III AUTOCAPTURE+
COFEPRIS Analysis ID: 954E2019 SSA
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Product Use / Uso del Producto
Spanish

EL PASADOR DE SUTURA FLEXIBLE EXPRESSEW® III AUTOCAPTURE+ ESTÁ INDICADO PARA PASAR SUTURAS A TRAVÉS DE TEJIDO EN INTERVENCIONES QUIRÚRGICAS ABIERTAS O ARTROSCÓPICAS.

English

EXPRESSEW® III AUTOCAPTURE+ FLEXIBLE SUTURE PIN IS INDICATED FOR PASSING SUTURES THROUGH TISSUE IN OPEN OR ARTHROSCOPIC SURGICAL PROCEDURES.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
PASADOR DE SUTURA FLEXIBLE
Trade Name (English)
FLEXIBLE SUTURE PIN
Registration Information
Analysis ID
954E2019 SSA
Registration Date
May 09, 2019
Manufacturer / Fabricante
Name (English)
JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.