• Acerca de la base de datos
  • ¿Cómo usar la IMDD?
  • Descargar la data
  • Preguntas frecuentes
  • Créditos
Vista de la lista Vista de las tarjetas
  • Dispositivo 500
  • Fabricante 31827
  • Evento 523
  • Implante 1
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall CLINITRON UPLIFT Physical Medicine Devices Hill-Rom Manufacturing, Inc. 2 United States USFDA
Device Recall PHS (Professional Hospital Supply) Physical Medicine Devices Rx Textiles Inc 1 United States USFDA
Device Recall Triton T700 Traction Unit Physical Medicine Devices Chattanooga Corp. United States USFDA
Device Recall Triton MP1 Traction Unit Physical Medicine Devices Chattanooga Corp. 1 United States USFDA
Device Recall Clinitron At Home Air Fluidized Therapy Unit Physical Medicine Devices Hill-Rom Manufacturing, Inc. 2 United States USFDA
Device Recall FLEXICAIR II Physical Medicine Devices Hill-Rom Manufacturing, Inc. 2 United States USFDA
Device Recall FLEXICAIR MC3 Physical Medicine Devices Hill-Rom Manufacturing, Inc. 2 United States USFDA
Device Recall Stryker 1550 Synergy Extended Stay Stretcher Physical Medicine Devices Stryker Medical 2 United States USFDA
Device Recall Tarsys 2G Tilt & Recline Seating System Physical Medicine Devices Invacare Corporation 2 United States USFDA
Device Recall Stryker 1050 hospital stretcher Physical Medicine Devices Stryker Medical 2 United States USFDA
Xact(tm) Drop Seat Base, a plastic seat support in Xact (tm) Integrated and Xact Individual w/ Drop seat Base Wheelchair cushions. Physical Medicine Devices Action Products Incorporated 1 United States USFDA
Device Recall KCI TriaDyne Proventa Physical Medicine Devices Kinetic Concepts, Inc 2 United States USFDA
Device Recall KCI Therapulse II Physical Medicine Devices Kinetic Concepts, Inc 2 United States USFDA
Device Recall KCI Physical Medicine Devices Kinetic Concepts, Inc 2 United States USFDA
Device Recall Lift Chairs Physical Medicine Devices Pride Mobility Products Corp 2 United States USFDA
VSP Shock Module (as part of a prosthetic foot). Physical Medicine Devices Ossur North America Inc 1 United States USFDA
iBOT 3000 Mobility System. Independence IBOT 3000 Mobility System (Stair-climbing wheelchair), Class III restricted medical device. The device is shipped one each per wooden pallet with wooden sides and top retained by reusable bands. Physical Medicine Devices Independence Technology LLC 2 United States USFDA
Device Recall Otto Bock 3R90 and 3R92 Single Axis Knee Joint Physical Medicine Devices Bock,Otto,Orthopedic Ind,Inc 1 United States USFDA
iBOT 3000 Mobility System, Independence iBOT 3000 Mobility System (Stair-climbing wheelchair), Class III restricted medical device. Physical Medicine Devices Independence Technology LLC 2 United States USFDA
Device Recall Victory Motorized Vehicle Physical Medicine Devices Pride Mobility Product Corp 2 United States USFDA
Device Recall Victory Motorized Vehicle Physical Medicine Devices Pride Mobility Product Corp 2 United States USFDA
Device Recall Cold Therapy Blanket Physical Medicine Devices DeRoyal Technologies Inc 2 United States USFDA
Device Recall Dermonosonic NonInvasive Subdermal Therapy System Physical Medicine Devices Sybaritic, Inc 2 United States USFDA
Device Recall ElectriCool II Physical Medicine Devices Cincinnati Sub-Zero Products Inc 2 United States USFDA
Device Recall Microtemp II. Physical Medicine Devices Cincinnati Sub-Zero Products Inc 2 United States USFDA
  • « First
  • ‹ Prev
  • …
  • 3
  • 4
  • 5
  • 6
  • 7
  • …
  • Next ›
  • Last »

Acerca de la base de datos

Explore más de 120,000 registros de retiros, alertas y notificaciones de seguridad de dispositivos médicos y sus conexiones con los fabricantes.

  • Preguntas frecuentes
  • Acerca de la base de datos
  • Contáctenos
  • Créditos

Historias en su correo

¿Trabaja en la industria médica? ¿O tiene experiencia con algún dispositivo médico? Nuestra reportería no ha terminado. Queremos oír de usted.

¡Cuéntanos tu historia!

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.