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  • Dispositivo 128
  • Fabricante 31827
  • Evento 155
  • Implante 27
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Pentax Ear, Nose, and Throat Devices Pentax Medical Company 2 United States USFDA
Pentax Ear, Nose, and Throat Devices Pentax Medical Company 2 United States USFDA
Pentax Ear, Nose, and Throat Devices Pentax Medical Company 2 United States USFDA
Alveolus Tracheobronchial Stent Technology System (TB-STS), Manufactured for: Alveolus Inc., 401 North Tryon Street, Charlotte, North Carolina USA 28202 Ear, Nose, and Throat Devices Alveolus, Inc. 2 United States USFDA
Device Recall Vision Sciences Battery Charger Ear, Nose, and Throat Devices Vision-Sciences, Inc. 2 United States USFDA
Device Recall Vision Sciences Battery Ear, Nose, and Throat Devices Vision-Sciences, Inc. 2 United States USFDA
Device Recall Airway balloon catheter Ear, Nose, and Throat Devices Acclarent, Inc. 2 United States USFDA
Device Recall SoundBite Microphone Tube Ear, Nose, and Throat Devices Sonitus Medical Inc. 2 United States USFDA
Device Recall SoundBite Microphone Tube Ear, Nose, and Throat Devices Sonitus Medical Inc. 2 United States USFDA
Device Recall SoundBite Microphone Tube Ear, Nose, and Throat Devices Sonitus Medical Inc. 2 United States USFDA
Device Recall SoundBite Microphone Tube Ear, Nose, and Throat Devices Sonitus Medical Inc. 2 United States USFDA
Device Recall SoundBite Microphone Tube Ear, Nose, and Throat Devices Sonitus Medical Inc. 2 United States USFDA
Device Recall BOMImed Reusable Integrated Fiber Optic Laryngoscope Blades Ear, Nose, and Throat Devices Bomimed Inc 2 United States USFDA
Device Recall BLOMSINGER indwelling TEP Occluder Ear, Nose, and Throat Devices Helix Medical LLC 2 United States USFDA
Device Recall WANG Transbronchial Aspiration Needles Ear, Nose, and Throat Devices ConMed Corporation 2 United States USFDA
Device Recall WANG Transbronchial Aspiration Needles Ear, Nose, and Throat Devices ConMed Corporation 2 United States USFDA
Device Recall WANG Transbronchial Aspiration Needles Ear, Nose, and Throat Devices ConMed Corporation 2 United States USFDA
Device Recall WANG Transbronchial Aspiration Needles Ear, Nose, and Throat Devices ConMed Corporation 2 United States USFDA
Device Recall Anspach Custom XMax Motor, Pneumatic with Hand Control and Custom Autolube III Ear, Nose, and Throat Devices The Anspach Effort, Inc. 2 United States USFDA
Device Recall Anspach Custom XMax Motor, Pneumatic Ear, Nose, and Throat Devices The Anspach Effort, Inc. 2 United States USFDA
Device Recall Anspach XMax Motor with Custom Hose Ear, Nose, and Throat Devices The Anspach Effort, Inc. 2 United States USFDA
Device Recall Inspira AIR Balloon Dilation system Ear, Nose, and Throat Devices Acclarent, Inc. 2 United States USFDA
Device Recall Inspira AIR Balloon Dilation system Ear, Nose, and Throat Devices Acclarent, Inc. 2 United States USFDA
Device Recall Inspira AIR Balloon Dilation system Ear, Nose, and Throat Devices Acclarent, Inc. 2 United States USFDA
Device Recall Inspira AIR Balloon Dilation system Ear, Nose, and Throat Devices Acclarent, Inc. 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.