FDA UDI In Commercial Distribution 🇺🇸 United States

Large Board

DI: B525BO030 · Model: BO-03 · Octostop Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Large Board
Primary DI
B525BO030
Version / Model
BO-03
Company Name
Octostop Inc
Labeler DUNS
240536946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-16
Public Version
4
Public Version Date
2019-05-23
Public Version Status
Update
Public Device Record Key
807750d2-153d-469c-9298-24f3ace4e6e5

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXH Cradle, patient, radiologic

GMDN Terms

Code Name
40902 Radiological whole-body positioner

Identifiers

Type ID
Primary B525BO030