FDA UDI Not in Commercial Distribution 🇺🇸 United States

EIT LLIF cage

DI: 04260557835005 · Model: LUI80940 · EIT Emerging Implant Technologies GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EIT LLIF cage
Primary DI
04260557835005
Version / Model
LUI80940
Company Name
EIT Emerging Implant Technologies GmbH
Labeler DUNS
313088331
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-27
Public Version
3
Public Version Date
2023-12-22
Public Version Status
Update
Public Device Record Key
3bdd150c-44d9-44e8-b1db-59e009069ff5
Distribution End Date
2023-02-15

Device Description

EIT LLIF, H 9mm, 8°, 40/22

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 Conditional
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 04260557835005