FDA UDI In Commercial Distribution 🇺🇸 United States

LUCENT

DI: 00840606116299 · Model: 13025-016 · SPINAL ELEMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUCENT
Primary DI
00840606116299
Version / Model
13025-016
Company Name
SPINAL ELEMENTS, INC.
Labeler DUNS
610712213
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-03
Public Version
5
Public Version Date
2021-02-11
Public Version Status
Update
Public Device Record Key
e4e96fe9-c642-4a2e-9684-609a9a50db94

Device Description

30MM X 25MM X 16MM CAGE 10°

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
Yes
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00840606116299

Customer Contacts