Mexico COFEPRIS registration 587C2020 SSA

MASCARILLA DE UN SOLO USOCOVALON

EN: SINGLE-USE MASKCOVALON
Mexico flagMexico·Clase I-Bajo Riesgo·V. SURGICAL AND HEALING MATERIALS·PROMESURGICAL, S.A. DE C.V.·Registered June 01, 2020
Product Use / Uso del Producto
Spanish

SE USA PARA REDUCIR EL RIESGO DETRANSFERENCIA DE PATÓGENOS ENTREINDIVIDUOS. ESTO SE LOGRA AL CUBRIR LASMEMBRANAS MUCOSAS DE LA NARIZ, LA BOCA Y LOS PULMONES CON LOS MATERIALES DEFILTRACIÓN DE LA MASCARILLA. LAMASCARILLA MÉDICA DE UN SOLO USO SEPUEDEUTILIZARCOMOPROTECCIÓNPARALOSINDIVIDUOS ASINTOMÁTICOS O PARACONTENER LAS GOTITAS DE INDIVIDUOSSINTOMÁTICOS.

English

IT IS USED TO REDUCE THE RISK OFTRANSFER OF PATHOGENS BETWEEN INDIVIDUALS. THIS IS ACHIEVED BY COVERING THE MUCOUS MEMBRANES OF THE NOSE, MOUTH AND LUNGS WITH THE DEFILTRATION MATERIALS OF THE MASK. THE SINGLE-USE MEDICAL MASK CAN BE USED AS PROTECTION FOR ASYMPTOMATIC INDIVIDUALS OR TO CONTAIN DROPLETS FROM SYMPTOMATIC INDIVIDUALS.

Device classification
Risk Class / Clase de Riesgo
Clase I-Bajo Riesgo
Product Type (Spanish)
V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
CUBREBOCAS
Trade Name (English)
MASK
Registration information
Analysis ID
587C2020 SSA
Registration Date
June 01, 2020
Manufacturer / Fabricante
Name (English)
PROMESURGICAL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for MASCARILLA DE UN SOLO USOCOVALON (SINGLE-USE MASKCOVALON) in the Mexico medical device market through Pure Global AI's free database. This Clase I-Bajo Riesgo medical device is registered under COFEPRIS analysis ID 587C2020 SSA and manufactured by PROMESURGICAL, S.A. DE C.V.. The device was registered on June 01, 2020.

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.

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