FDA UDI In Commercial Distribution 🇺🇸 United States

ROI-A

DI: 03662663011310 · Model: IR2526P · LDR Spine Usa, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROI-A
Primary DI
03662663011310
Version / Model
IR2526P
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
15ae7a32-8c4e-4417-bbde-509b3ffb5ba2

Device Description

ROI-A MEDIAN IMPLANT PXL 27X30 H14 6°

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
MQP Spinal Vertebral Body Replacement Device
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 03662663011310

Customer Contacts

Phone
512-344-3333

Device Sizes

Type Value Unit Text
Angle 6 degree
Width 30 Millimeter
Depth 27 Millimeter
Height 14 Millimeter