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  • Dispositivo 374
  • Fabricante 58
  • Evento 124969
  • Implante 1
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall CAPSure; Coblator; CoVAC; ArthroWand; Microblastor; Saber; Saphyre; SERFAS; TriStar; VARP; Vulcan. General and Plastic Surgery Devices Surgical Instrument Service And Savings, Inc. 2 United States USFDA
Device Recall Central Line Dressing Change Tray General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall Central Line Dressing Change Tray General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall Centurion General Hospital and Personal Use Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall Centurion C.A.P.D. Tubing Exchange Tray Gastroenterology-Urology Devices Centurion Medical Products 1 United States USFDA
Device Recall CENTURION CENTAL LINE ACCESSORY PACK General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL CATHETER INSERTION TRAY General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE INSERTION TRAY General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE PROCEDURE KIT General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL LINE PROCEDURE TRAY General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CENTRAL VENOUS CATHETERIZATION BUNDLE TRAY General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CHARLES COLE CVC INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall Centurion Convenience Kits General Hospital and Personal Use Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC ACCESSORY KIT General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC MULTI LUMEN INSERTIN BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC MULTILUMEN INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC MULTILUMEN INSERTION BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC TRIPLE LUMEN BUNDLE General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC TRIPLE LUMEN BUNDLE, 7FR/16CM General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC TRIPLE LUMEN BUNDLE KIT General and Plastic Surgery Devices Centurion Medical Products Corporation 2 United States USFDA
Device Recall CENTURION CVC TRIPLE LUMEN KIT General and Plastic Surgery Devices Centurion Medical Products Corporation 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.