FDA UDI In Commercial Distribution 🇺🇸 United States

BeamSite

DI: 00860009184503 · Model: BeamSite · Doseoptics LLC
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BeamSite
Primary DI
00860009184503
Version / Model
BeamSite
Company Name
Doseoptics LLC
Labeler DUNS
079605332
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-10
Public Version
1
Public Version Date
2023-08-18
Public Version Status
New
Public Device Record Key
bd9ab582-3372-4f8e-a772-7ff0ee63468f

Device Description

BeamSite™ is a camera system that enables live visualization of the treatment beam on a patient during radiotherapy. It is an optically based system that is non-patient contacting and produces no radiation. When the treatment beam is on, BeamSite captures images of Cherenkov light emitted from the patient’s skin during radiotherapy to provide an optical map of the treatment beam on the patient. When the treatment beam is off, the system provided continuous background images of the treatment area under ambient light illumination. The BeamSite system consists of a camera, a workstation with preinstalled BeamSite software, and a monitor to be used by clinical radiotherapy teams to a) visually observe the patient and the Cherenkov light emitted from irradiated surface anatomy, and b) review the treatment images, if necessary.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
40887 Radiation therapy software
40942 Radiation therapy system workstation, multi-purpose

Identifiers

Type ID
Primary 00860009184503

Premarket Submissions

Submission Number Supplement Number
K212606 000