CATÉTER URETERAL PROMEDON - COFEPRIS Registration 1946C2021 SSA
Access comprehensive regulatory information for CATÉTER URETERAL PROMEDON (PROMEDON URETERAL CATHETER) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1946C2021 SSA and manufactured by PROMESURGICAL, S.A.DE C.V.. The device was registered on November 24, 2021.
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.
EL CATÉTER URETERAL PROMEDON ES UNPRODUCTODEUNSOLOUSOQUESEEMPLEAPARA DRENAJE O PIELOGRAMARETRÓGRADO.SEUTILIZAPARAESTABLECERUN CONDUCTO HACIA EL URÉTER Y ASÍPODER REALIZAR LA INYECCIÓN DE MEDIODE CONTRASTE, INTERCAMBIO DE CABLEGUÍA, ETC. INDICADO PARA: DRENAJEURINARIOTEMPORAL,URETEROPIELOGRAFÍARETRÓGRADA, OPACIFICACIÓN DEL SISTEMACOLECTOR PARA EL ACCESO PERCUTÁNEO,AYUDAPARAOBTENERACCESOALORIFICIOURETERAL,CAMBIARCABLEGUÍAS,OBTENERCITOLOGÍA Y CEPILLADO URINARIO DE
THE PROMEDON URETERAL CATHETER IS A SINGLE-USE PRODUCT USED FOR DRAINAGE OR RETROGRADE PYELOGRAM. IT IS USED TO ESTABLISH A CONDUIT TO THE URETER AND THUS BE ABLE TO PERFORM THE INJECTION OF CONTRAST MEDIUM, EXCHANGE OF CABLEGUIDE, ETC. INDICATED FOR: TEMPORAL URINARY DRAINAGE,URETEROPYELOGRAPHYRETROGRADE, OPACIFICATION OF THE COLLECTING SYSTEM FOR PERCUTANEOUS ACCESS,HELP TO OBTAIN ACCESS TO URETERAL ORIFICE,CHANGECABLEGUIDES,OBTAIN CYTOLOGY AND URINARY BRUSHING OF

