FDA UDI In Commercial Distribution 🇺🇸 United States

FI-Kit

DI: B525FIKIT0 · Model: FI-KIT · Octostop Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FI-Kit
Primary DI
B525FIKIT0
Version / Model
FI-KIT
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
f6f1b475-41d4-4f5f-9a3e-493872319dd2

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
KPR System, x-ray, stationary

GMDN Terms

Code Name
37692 X-ray/radiation therapy beam filter, wedge

Identifiers

Type ID
Primary B525FIKIT0