MEVION S250-FIT Proton Therapy System (UDI S250-FIT)
Manufactured by MEVION MEDICAL SYSTEMS, INC.
Device Regulatory Overview
The MEVION S250-FIT Proton Therapy System (Model/Catalog Number: S250-FIT) is a medical device manufactured by MEVION MEDICAL SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification LHN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S250-FIT
- Product Code / EMDN
- LHN
- Device Name
- he MEVION S250-FIT Proton Beam Radiation Therapy Device is intended to deliver proton radiation treatment to patients with localized tumors or any other conditions susceptible to treatment by radiation. When the patient is in the fully seated position, the MEVION S250-FIT is indicated for treatment of patients with localized tumors and other conditions susceptible to treatment by radiation in the sites above the mid-chest or carina.
- Database Sync Date
- 2026-08-09 09:49:15
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MEVION S250-FIT Proton Therapy System?
The registered manufacturer of record for MEVION S250-FIT Proton Therapy System is MEVION MEDICAL SYSTEMS, INC..
What is the Primary UDI-DI identifier for MEVION S250-FIT Proton Therapy System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S250-FIT.
What classification code is assigned to this device?
This device is registered under product classification code LHN.
Similar Classification Devices (LHN)
Other Devices by MEVION MEDICAL SYSTEMS, INC.
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