Devices

Device Recall Proteus 325

Model / Serial
Proteus 235 Proton Therapy System Legacy Software version 7.2.7 and higher, models 110, 112, 113, and 116.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US Distribution including the states of OK, IL, NJ, and WA.
Product Description
Proteus 235 Proton Therapy System Legacy Software version 7.2.7 and higher, models 110, 112, 113, and 116. || Proton therapy
Manufacturer
Ion Beam Applications S.A.
1 Event
- Recall of Device Recall Proteus 325

Manufacturer

Ion Beam Applications S.A.

Manufacturer Address
Ion Beam Applications S.A., Chemin du Cyclotron, 3, Louvain La Neuve Belgium
Manufacturer Parent Company (2017)
Ion Beam Applications SA
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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