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  • Dispositivo 128
  • Fabricante 31827
  • Evento 155
  • Implante 27
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Cochlear Nucleus Sterile Silicone Template Ear, Nose, and Throat Devices Cochlear Americas Inc. 3 United States USFDA
Auria PowerPak, Model CI-7400-xxx where xxx denotes color/cable length options. Ear, Nose, and Throat Devices Advanced Bionics Corporation 3 United States USFDA
Device Recall HiResolution Bionic Ear System Ear, Nose, and Throat Devices Advanced Bionics Corporation 3 United States USFDA
Device Recall HiResolution Bionic Ear System Ear, Nose, and Throat Devices Advanced Bionics Corporation 3 United States USFDA
Total Ossicular Replacement Prosthesis, CliP Piston MVP Ear, Nose, and Throat Devices Heinz Kurz GmbH Medizintechnik 2 United States USFDA
CLARION 1.2, Advanced Bionics implantable cochlear stimulator Ear, Nose, and Throat Devices Advanced Bionics 3 United States USFDA
CLARION CII, Advanced Bionics implantable cochlear stimulator Ear, Nose, and Throat Devices Advanced Bionics 3 United States USFDA
HiRes 90, Model CI140001, Advanced Bionics implantable cochlear stimulator Ear, Nose, and Throat Devices Advanced Bionics 3 United States USFDA
NUCLEUS COCHLEAR IMPLANT SYSTEM Ear, Nose, and Throat Devices Cochlear Americas Inc. 3 United States USFDA
Device Recall Esteem Programmers Ear, Nose, and Throat Devices Envoy Medical Corporation 3 United States USFDA
Device Recall Universal Titanium Prosthesis, Ear, Nose, and Throat Devices Medtronic Xomed, Inc. 2 United States USFDA
Device Recall Armstrong Grommet Ear, Nose, and Throat Devices Summit Medical, Inc. 2 United States USFDA
Device Recall HiRes90K Platinum Series Headpiece Ear, Nose, and Throat Devices Advanced Bionics LLC 3 United States USFDA
Device Recall Platinum Series Headpiece Ear, Nose, and Throat Devices Advanced Bionics LLC 3 United States USFDA
Device Recall SSeries Headpiece Long Range Ear, Nose, and Throat Devices Advanced Bionics LLC 3 United States USFDA
Device Recall SSeries Headpiece Short Range Ear, Nose, and Throat Devices Advanced Bionics LLC 3 United States USFDA
Device Recall Harmony HiResolution Bionic Ear system Ear, Nose, and Throat Devices Advanced Bionics LLC 3 United States USFDA
Device Recall Micron Bobbin Vent Tube Ear, Nose, and Throat Devices Gyrus ACMI Corporation 2 United States USFDA
Device Recall SP78100, SP78105 Nasal Septal Button Standard (3cm) Ear, Nose, and Throat Devices Micromedics, Inc. Unclassified United States USFDA
Device Recall VT010150 Otological Ventilation Tubes Ear, Nose, and Throat Devices Micromedics, Inc. 2 United States USFDA
Device Recall Advanced Bionics HiRes 90K Cochlear Implant device Ear, Nose, and Throat Devices Advanced Bionics Corporation 3 United States USFDA
Device Recall Advanced Bionics HiRes 90K Cochlear Implant device Ear, Nose, and Throat Devices Advanced Bionics Corporation 3 United States USFDA
Cochlear Nucleus CI512 Cochlear Implant Ear, Nose, and Throat Devices Cochlear Americas Inc. 3 United States USFDA
HiRes 90K Ear, Nose, and Throat Devices Advanced Bionics Corporation 3 United States USFDA
PARPARELLATYPE VENT TUBE, 1.02 MM Ear, Nose, and Throat Devices Gyrus Acmi, Incorporated 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.