Devices

Device Recall Proteus 235

Model / Serial
PAT.107, PAT.109, PAT.112, PAT.113, PAT.114, PAT.115, PAT.116, PAT.119.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide) including the states of PA, NJ, IL, WA, and TN, and the countries of Germany, Italy, and Czech Republic.
Product Description
Proteus 235 || Proton Therapy System for cancer treatment.
Manufacturer
Ion Beam Applications S.A.
1 Event
- Recall of Device Recall Proteus 235

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

One device with a similar name

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Device Recall Proteus 235 and Proteus ONE proton therapy systems

Model / Serial
Code/Serial Numbers: PAT.003, PAT.006, PAT.107, PAT.108, PAT.109, PAT.110, PAT.111, PAT.112, PAT.113, PAT.114, PAT.115, SAT.116, SAT.117, SAT.119, SAT.120, SAT.122, SAT.123 and SAT.126
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Products distributed to FL, VA, PA, OK, IL, NJ, WA, TN, LA, TX, South Korea, Germany, France, Czech Republic, Italy, Poland, and Sweden
Product Description
Proteus 235 and Proteus ONE proton therapy systems
Manufacturer
Ion Beam Applications S.A.

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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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