The Implant Files -
International Medical Devices Database
- About this investigation
- International Medical Devices Database
- Tell us your story
- Resources for patients
- Reporting partners
- Video introduction
Historias - Patients harmed by medical devices
- Europe, a device gateway to the world
- History of the industry
- The Medtronic way
- Ruptured trust and breast implants
- Heart device raises risk questions
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Modelo / Serial
- Manufacturer
- 1 Event
Fabricante
- Empresa matriz del fabricante (2017)
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Comentario del fabricante
Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
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Source
IGJ
10 dispositivos con un nombre similar
Más información acerca de la data acá
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Modelo / Serial
Model: 900-600; 900-601; 900-602, Affected: Various Lot numbers
- Manufacturer
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Modelo / Serial
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Descripción del producto
md
- Manufacturer
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Modelo / Serial
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Descripción del producto
medical_device
- Manufacturer
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Modelo / Serial
- Manufacturer
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Modelo / Serial
Catalog Number: 900-600, 900-601 & 900-602
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Descripción del producto
Medical devices for single use
- Manufacturer