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CATÉTER URETERAL HIDRÓFILO - COFEPRIS Registration 1356C2024 SSA

Access comprehensive regulatory information for CATÉTER URETERAL HIDRÓFILO (CATÉTER URETERAL HIDRÓFILO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1356C2024 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on May 09, 2024.

This page provides complete registration details including product type (V. Materiales quirúrgicos y de curación), 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
1356C2024 SSA
CATÉTER URETERAL HIDRÓFILO
COFEPRIS Analysis ID: 1356C2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
V. Materiales quirúrgicos y de curación
Product Type (English)
V. Materiales quirúrgicos y de curación
Trade Name (Spanish)
BD READY-TO-USE HYDROPHILIC CATHETER
Trade Name (English)
BD READY-TO-USE HYDROPHILIC CATHETER
Registration Information
Analysis ID
1356C2024 SSA
Registration Date
May 09, 2024
Manufacturer / Fabricante
Name (English)
BECTON DICKINSON DE MÉXICO, S.A. DE C.V.