CLEARVUE 350/550
Mexico·Clase II·I. MEDICAL EQUIPMENT·PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.·Registered February 02, 2018DISPOSITIVO DISEÑADO PARA EL DIAGNÓSTICO POR EL ULTRASONIDO MEDIANTE IMAGEN
DEVICE DESIGNED FOR ULTRASOUND IMAGING
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- SISTEMA DE ULTRASONIDO
- Trade Name (English)
- ULTRASOUND SYSTEM
- Analysis ID
- 305E2018 SSA
- Registration Date
- February 02, 2018
- Name (Spanish)
- PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.
- Name (English)
- PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.
Access comprehensive regulatory information for CLEARVUE 350/550 (CLEARVUE 350/550) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 305E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on February 02, 2018.
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.