FDA UDI In Commercial Distribution 🇺🇸 United States

Octane Straight

DI: 10885862235992 · Model: 05-071-03-2812 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Octane Straight
Primary DI
10885862235992
Version / Model
05-071-03-2812
Catalog Number
05-071-03-2812
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-30
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
6af560e4-a75a-43a3-b961-9239a9da147c

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 10885862235992

Device Sizes

Type Value Unit Text
Width 28 Millimeter
Length 10 Millimeter
Height 12 Millimeter
Device Size Text, specify Lordotic