FDA UDI In Commercial Distribution 🇺🇸 United States

E3D-A Interbody System

DI: 00195860019948 · Model: 111-A40282019 · Evolution Spine LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
E3D-A Interbody System
Primary DI
00195860019948
Version / Model
111-A40282019
Catalog Number
111-A40282019
Company Name
Evolution Spine LLC
Labeler DUNS
116940934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-15
Public Version
1
Public Version Date
2023-03-23
Public Version Status
New
Public Device Record Key
1a78374b-c65e-4dea-9eab-ec6e152da10b

Device Description

ALIF TRIAL 40 X 28mm 20deg 19mm (P 9 mm)

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
No
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00195860019948

Customer Contacts