FDA UDI In Commercial Distribution 🇺🇸 United States

Scarlet AL-T Instruments

DI: 07640185348479 · Model: SPE-US M5 12-N · SpineArt SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Scarlet AL-T Instruments
Primary DI
07640185348479
Version / Model
SPE-US M5 12-N
Catalog Number
SPE-US M5 12-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-29
Public Version
1
Public Version Date
2021-04-06
Public Version Status
New
Public Device Record Key
63c2c2c0-b619-4181-8332-626f55337ce5

Device Description

SMOOTH TRIAL Medium

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 07640185348479

Device Sizes

Type Value Unit Text
Height 12 Millimeter
Angle 15 degree