FDA UDI In Commercial Distribution 🇺🇸 United States

Gemini360RT

DI: 00860014221903 · Model: Gemini360RT · Akesis Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gemini360RT
Primary DI
00860014221903
Version / Model
Gemini360RT
Company Name
Akesis Inc.
Labeler DUNS
081307120
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-15
Public Version
1
Public Version Date
2025-08-25
Public Version Status
New
Public Device Record Key
95ae0a24-85cc-4489-9df4-d71a0d0b1412

Device Description

The Akesis Gemini360RT is a radiation therapy system based on a LINAC platform with an optional Gamma head for multimodal treatment delivery.

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
No
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
35159 Linear accelerator system

Identifiers

Type ID
Primary 00860014221903

Premarket Submissions

Submission Number Supplement Number
K210921 000