Mexico COFEPRIS registration 2019E2019 SSA

ENDOFAST VT GUIDE

EN: ENDOFAST VT GUIDE
Mexico flagMexico·Clase I·I. MEDICAL EQUIPMENT·LEVBETH MEDICAL, S.A. DE C.V.·Registered October 21, 2019
Product Use / Uso del Producto
Spanish

LA ENDOFAST VT GUIDE HA SIDO DISEÑADA PARA RETRACCIÓN DURANTE PROCEDIMIENTOS QUIRÚRGICOS TRANSVAGINALES, COMO LA REPARACIÓN QUIRÚRGICA ANTERIOR Y POSTERIOR DEL PROLAPSO PÉLVICO DEL ÓRGANO.

English

THE ENDOFAST VT GUIDE HAS BEEN DESIGNED FOR RETRACTION DURING TRANSVAGINAL SURGICAL PROCEDURES, SUCH AS ANTERIOR AND POSTERIOR SURGICAL REPAIR OF PELVIC ORGAN PROLAPSE.

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
RETRACTOR EN FORMA DE S
Trade Name (English)
S-SHAPED RETRACTOR
Registration information
Analysis ID
2019E2019 SSA
Registration Date
October 21, 2019
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for ENDOFAST VT GUIDE (ENDOFAST VT GUIDE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2019E2019 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on October 21, 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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