FDA UDI In Commercial Distribution 🇺🇸 United States

SpF®-PLUS-Mini (60 uA/W)

DI: 00812301020133 · Model: 10-1398W · EBI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpF®-PLUS-Mini (60 uA/W)
Primary DI
00812301020133
Version / Model
10-1398W
Catalog Number
10-1398W
Company Name
EBI, LLC
Labeler DUNS
050410323
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-19
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
5809fb58-20de-4476-b6cf-16ad16f58da5

Device Description

SPF-PLUS 60/W Implantable Spinal Fusion Stimulator

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LOE Stimulator, Invasive Bone Growth

GMDN Terms

Code Name
35463 Patient-worn bone growth electromagnetic stimulator

Identifiers

Type ID
Primary 00812301020133

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P850035 033

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 77 Degrees Fahrenheit