FDA UDI In Commercial Distribution 🇺🇸 United States

CERES

DI: 00840916127374 · Model: 12-30-0357 · SPINAL ELEMENTS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CERES
Primary DI
00840916127374
Version / Model
12-30-0357
Company Name
SPINAL ELEMENTS
Labeler DUNS
004022104
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-18
Public Version
8
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
c952e8a9-3c8b-4409-a853-1aaa6d3c2e62

Device Description

Ceres® 3-Level, 57mm Cervical Plate

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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00840916127374