FDA UDI In Commercial Distribution 🇺🇸 United States

OMNI

DI: 00840916107192 · Model: CT05045 · SPINAL ELEMENTS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OMNI
Primary DI
00840916107192
Version / Model
CT05045
Company Name
SPINAL ELEMENTS
Labeler DUNS
004022104
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-19
Public Version
5
Public Version Date
2020-12-17
Public Version Status
Update
Public Device Record Key
35ef0b5e-49ca-4999-ab1a-d2851417fd3e

Device Description

5.0mm x 45mm Cannulated Screw

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00840916107192