FDA UDI In Commercial Distribution 🇺🇸 United States

SCARLET AL-T INSTRUMENTATION

DI: 07640185347601 · Model: SCA-TS 20 19-N · SpineArt SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCARLET AL-T INSTRUMENTATION
Primary DI
07640185347601
Version / Model
SCA-TS 20 19-N
Catalog Number
SCA-TS 20 19-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-29
Public Version
1
Public Version Date
2020-02-06
Public Version Status
New
Public Device Record Key
e9e16c03-f398-4aa2-ae76-7a9ed1c3b8c9

Device Description

TRIAL SMALL

Device Characteristics

Single Use
No
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
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 07640185347601

Device Sizes

Type Value Unit Text
Height 19 Millimeter
Angle 20 degree