FDA UDI In Commercial Distribution 🇺🇸 United States

MOBIO™ Total Knee System

DI: 00843575111159 · Model: 8829301212 · B-ONE ORTHO, CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MOBIO™ Total Knee System
Primary DI
00843575111159
Version / Model
8829301212
Catalog Number
8829301212
Company Name
B-ONE ORTHO, CORP.
Labeler DUNS
081315444
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-18
Public Version
2
Public Version Date
2022-03-22
Public Version Status
Update
Public Device Record Key
f93f459d-8322-4558-a3a7-7999d5749e67

Device Description

CR PLUS Tibial Insert Trial, Size A/1-3+, 12mm

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
Yes
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 00843575111159