FDA UDI In Commercial Distribution 🇺🇸 United States

LUCENT L

DI: 00840606145121 · Model: 80002-000-05 · SPINAL ELEMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUCENT L
Primary DI
00840606145121
Version / Model
80002-000-05
Company Name
SPINAL ELEMENTS, INC.
Labeler DUNS
610712213
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-25
Public Version
4
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
8ddf9af8-9d48-4d3f-894d-15e0f66e82f5

Device Description

LUCENT® LATERAL INSTRUMENTS TRAY MIDDLE INSERT

Device Characteristics

Single Use
No
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
Yes
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
OJH Orthopedic Tray

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 00840606145121