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Proteus 235

FDA UDI

Class II (US FDA UDI)

by Ion Beam Applications SA

Identity

Trade Name
Proteus 235 FDA UDI
Generic Name
Proton therapy system FDA UDI
Device Name
IBA Proton Therapy System – Proteus 235 FDA UDI
Model / Reference
Proteus PLUS FDA UDI
Description
IBA Proton Therapy System – Proteus 235 FDA UDI

Identifiers

Catalog Number
NA FDA UDI
Primary DI / UDI-DI
05404013813308 FDA UDI
FDA Product Code
LHN FDA UDI
GMDN Term
Proton therapy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Proton therapy system

Proteus 235 by Ion Beam Applications SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Proton therapy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 92b5b587-8091-4550-8dd2-38d26ee86e5c 34 fields · synced Jun 8, 2026