FDA UDI In Commercial Distribution 🇺🇸 United States

Sapphire X3

DI: 00840606178228 · Model: 27081-014 · SPINAL ELEMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sapphire X3
Primary DI
00840606178228
Version / Model
27081-014
Company Name
SPINAL ELEMENTS, INC.
Labeler DUNS
610712213
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-02
Public Version
1
Public Version Date
2024-02-12
Public Version Status
New
Public Device Record Key
d18a0a1b-deb3-47bc-a0c4-90575ad777e4

Device Description

1-LEVEL SAPPHIRE X3, 14MM, 17.5MM WIDE

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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00840606178228