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  • Dispositivo 128
  • Fabricante 31827
  • Evento 155
  • Implante 27
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
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
Boston Scientific brand Microbiology Specimen Brush, single use, sterile, 220 cm, package of 10 brushes; Catalog No. 1640, Order No. M00516401. Ear, Nose, and Throat Devices Boston Scientific Corp 2 United States USFDA
Boston Scientific brand Microbiology Specimen Brush, single use, sterile, 90 cm, package of 10 brushes; Catalog No. 1650, Order No M00516501. Ear, Nose, and Throat Devices Boston Scientific Corp 2 United States USFDA
Brand name: || NIM¿ EMG Endotracheal Tube REF 82-29106, 82-29107, 82-29108 || NIM¿ EMG Reinforced Endotracheal Tube REF 82-29306, 82-29307, 82-29308 || [All products are packaged one unit per box.] Ear, Nose, and Throat Devices Medtronic Xomed, Inc. 2 United States USFDA
Celerity PICC Tip Confirmation System Ear, Nose, and Throat Devices Angiodynamics Inc. (Navilyst Medical Inc.) 1 United States USFDA
Cochlear Baha Soft tissue gauge Ear, Nose, and Throat Devices Cochlear Americas Inc. 2 United States USFDA
Device Recall 2.0x7mm Fossa Xdrive screws Ear, Nose, and Throat Devices Biomet Microfixation, Inc. 1 United States USFDA
Device Recall Acclarent Ear, Nose, and Throat Devices Acclarent Inc 1 United States USFDA
Device Recall Airway balloon catheter Ear, Nose, and Throat Devices Acclarent, Inc. 2 United States USFDA
Device Recall ALGO Newborn Hearing screener Ear, Nose, and Throat Devices Natus Medical 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 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 MIA 16 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 AquaStar Ear, Nose, and Throat Devices Micromedical Technologies, Inc 1 United States USFDA
Device Recall Bivona Laryngectomy Tube Ear, Nose, and Throat Devices Smiths Medical ASD, Inc. 1 United States USFDA
Device Recall BlackMax Motor System Ear, Nose, and Throat Devices The Anspach Effort, Inc. 2 United States USFDA
Device Recall BlomSinger Adjustable Tracheostoma Valve II Ear, Nose, and Throat Devices Helix Medical LLC 2 United States USFDA
Device Recall BLOMSINGER indwelling TEP Occluder Ear, Nose, and Throat Devices Helix Medical LLC 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 Boston Medical Products Inc (OEM) Ear, Nose, and Throat Devices Ultracell Medical Technologies 1 United States USFDA
Device Recall Boston Medical Products Inc (OEM) Ear, Nose, and Throat Devices Ultracell Medical Technologies 1 United States USFDA
Device Recall Boston Scientific SpyGlass Light Cable Ear, Nose, and Throat Devices Boston Scientific Corporation 1 United States USFDA
Device Recall CORE Universal Driver Ear, Nose, and Throat Devices Stryker Instruments Div. of Stryker Corporation 2 United States USFDA
Device Recall Customed Ear, Nose, and Throat Devices Customed, Inc 1 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.