FDA UDI Not in Commercial Distribution 🇺🇸 United States

BIONIX RADIATION THERAPY

DI: 00817740020119 · Model: UTRT-5012A · Bionix Radiation Therapy, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIONIX RADIATION THERAPY
Primary DI
00817740020119
Version / Model
UTRT-5012A
Catalog Number
UTRT-5012A
Company Name
Bionix Radiation Therapy, LLC
Labeler DUNS
080397923
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-25
Public Version
5
Public Version Date
2023-07-10
Public Version Status
Update
Public Device Record Key
1c629fbe-ae57-4e6e-a55b-22bd225074e4
Distribution End Date
2020-10-30

Device Description

SECURE FIT BAR: HEAD AND NECK

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
Yes
PM Exempt
No
Has Serial Number
No
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
40895 Vacuum-mould patient positioning system

Identifiers

Type ID
Primary 00817740020119

Customer Contacts