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  • Dispositivo 3821
  • Fabricante 31827
  • Evento 4589
  • Implante 424
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall 9F Plastic Dual Port General Hospital and Personal Use Devices Medical Components, Inc dba MedComp 2 United States USFDA
Device Recall Codman 3000 Series Refill Set General Hospital and Personal Use Devices Codman & Shurtleff, Inc. 3 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall Celsite Implantable Access Port System General Hospital and Personal Use Devices B. Braun Interventional Systems 2 United States USFDA
Device Recall Bard Access Marketing Brochures General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall Arrow Intl PICC Kits with PeelAway Sheath Component General Hospital and Personal Use Devices Arrow International Inc 2 United States USFDA
Device Recall Ascenda Intrathecal Catheter Model 8781 General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Vaxcel PICC with PASV Catheter Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Vaxcel PICC with PASV Introducer Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Vaxcel PICC with PASV IR145 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Vaxcel PICC with PASV MST30 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Vaxcel PICC with PASV MST60 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Vaxcel PICC with PASV Introducer Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Vaxcel PICC with PASV Intermediate Safety MST Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela PICC with PASV Valve Technology Catheter Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela PICC with PASV Valve Technology, IR145 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela PICC with PASV Valve Technology General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela PICC with PASV Valve Technology, Intermediate MST45 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela Hybrid PICC with PASV Valve Technology, Catheter Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela Hybrid PICC with PASV Valve Technology, IR145 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela Hybrid PICC with PASV Valve Technology, MST70 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
Device Recall Xcela Hybrid PICC with PASV Valve Technology, Intermediate MST45 Kit General Hospital and Personal Use Devices Navilyst Medical, Inc., an AngioDyamics Company 2 United States USFDA
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.