FDA UDI In Commercial Distribution 🇺🇸 United States

ROI-T

DI: 03662663041515 · Model: IR9131R · LDR Spine Usa, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROI-T
Primary DI
03662663041515
Version / Model
IR9131R
Catalog Number
IR9131R
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-09
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
f132ac24-a39a-48b1-b1d3-9b348e12b357

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 03662663041515

Customer Contacts

Phone
800-699-3360

Device Sizes

Type Value Unit Text
Height 13 Millimeter