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  • Dispositivo 124
  • Fabricante 32
  • Evento 124969
  • Implante 6
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Kii Shielded Bladed Access System and Kii Low Profile System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Voyant Open Fusion Device General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Applied Medical's Inzii 12/15mm Retrieval System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Applied Medical Kii Optical Access System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Epix and Direct Drive Laparoscopic Graspers Obstetrical and Gynecological Devices Applied Medical Resources Corp 1 United States USFDA
Device Recall Kii Shielded Bladed Access System Clinical Chemistry and Clinical Toxicology Devices Applied Medical Resources Corp 1 United States USFDA
Device Recall Applied Medical Kii Optical Access System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Applied Medical Kii Optical Access System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Applied Medical Kii Optical Access System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Applied Medical Kii Optical Access System General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Surgical Clamp Inserts Cardiovascular Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Surgical Clamp Inserts Cardiovascular Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Surgical Clamp Inserts Cardiovascular Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Direct Drive Grasper General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Direct Drive Grasper General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Direct Drive Grasper General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Irrigation Catheters Cardiovascular Devices Applied Medical Resources Corp 2 United States USFDA
Embolectomy Catheters Cardiovascular Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Lap Banding Kit General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Lap Banding Kit General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall Lap Banding Kit General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall 15mm Separator Access System Obstetrical and Gynecological Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall 15mm Separator Access System Obstetrical and Gynecological Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall 15mm Separator Access System Obstetrical and Gynecological Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall 15mm Separator Access System Obstetrical and Gynecological Devices Applied Medical Resources Corp 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.