Proteus 235

GUDID 05404013821303

IBA Proton Therapy System – Proteus 235

Ion Beam Applications SA

Proton therapy system

• Primary Device ID: 05404013821303
• NIH Device Record Key: 24bc9cc1-d8a5-455c-af9b-3df1e431f1d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Proteus 235
• Version Model Number: Proteus ONE
• Company DUNS: 372078154
• Company Name: Ion Beam Applications SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05404013821303 [Primary]

FDA Product Code

• LHN: System, Radiation Therapy, Charged-Particle, Medical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-28

On-Brand Devices [Proteus 235]

• 05404013821303: IBA Proton Therapy System – Proteus 235
• 05404013820504: IBA Proton Therapy System – Proteus 235
• 05404013814015: IBA Proton Therapy System – Proteus 235
• 05404013813308: IBA Proton Therapy System – Proteus 235
• 05404013810901: IBA Proton Therapy System – Proteus 235