FDA UDI In Commercial Distribution 🇺🇸 United States

CURE LP

DI: 07640270061764 · Model: S2-9-41355-25 · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CURE LP
Primary DI
07640270061764
Version / Model
S2-9-41355-25
Catalog Number
S2-9-41355-25
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-17
Public Version
1
Public Version Date
2025-11-25
Public Version Status
New
Public Device Record Key
ac676d12-8c9b-4b2b-8232-2d569e97c9a3

Device Description

LUMBAR FIXED SELF TAPPING SCREW (x2) Ø5.5 L25

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 07640270061764