FDA UDI In Commercial Distribution 🇺🇸 United States

SCARLET AL-T

DI: 07640375235718 · Model: SPE-US 01 41-N · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCARLET AL-T
Primary DI
07640375235718
Version / Model
SPE-US 01 41-N
Catalog Number
SPE-US 01 41-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-14
Public Version
1
Public Version Date
2022-10-24
Public Version Status
New
Public Device Record Key
e78f0dc4-f4e3-44aa-a778-1fb542146fee

Device Description

UNIVERSAL IMPLANT INSERTER

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
Yes
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
HWR Driver, Prosthesis

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 07640375235718