FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kobold® SBRT Board

DI: 00815568020243 · Model: 300-000 · KOBOLD, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kobold® SBRT Board
Primary DI
00815568020243
Version / Model
300-000
Company Name
KOBOLD, LLC
Labeler DUNS
014292258
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2019-08-19
Public Version Status
Update
Public Device Record Key
fe9c29f4-261f-43f6-9866-a70e2247fc0a
Distribution End Date
2019-07-26

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
Yes
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
KXJ Table, Radiologic

GMDN Terms

Code Name
40897 Indexed-immobilization patient positioning system

Identifiers

Type ID
Primary 00815568020243