FDA UDI In Commercial Distribution 🇺🇸 United States

Avenue L

DI: 03662663040068 · Model: IR90069R · LDR Spine Usa, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Avenue L
Primary DI
03662663040068
Version / Model
IR90069R
Catalog Number
IR90069R
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-22
Public Version
6
Public Version Date
2022-11-07
Public Version Status
Update
Public Device Record Key
df6278d3-cb15-4d8e-9f0f-e2493d66fa72

Device Description

TRIAL H12MM 17X50MM 10°

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
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 03662663040068

Customer Contacts

Phone
800-699-3360

Device Sizes

Type Value Unit Text
Width 50 Millimeter
Height 12 Millimeter
Depth 17 Millimeter
Angle 10 degree